I am grateful to Marc Ridilla (Repair Biotechnologies) and Brian Haarer (SUNY Upstate) for helpful comments on this protocol. This work was supported by the National Institutes of Health (GM133485).

1. Washing the coverslips
NOTE: Wash (24 mm x 60 mm, #1.5) coverslips according to Smith et al., 201328.
<ol>
	<li>Arrange coverslips in a plastic slide mailer container.</li>
	<li>Submerge coverslips sequentially in the following solutions and sonicate for 30-60 min, rinsing with ddH2O 10 times in between each solution: ddH2O with one drop of dish soap; 0.1 M KOH. Store coverslips in 100% ethanol for up to 6 months. 
	NOTE: Do not touch glass surfaces with ungloved fingers. Use forceps instead.</li>
</ol>
2. Coating cleaned (24 mm x 60 mm, #1.5) coverslips with mPEG- and biotin-PEG-silane
NOTE: This protocol specifically uses a biotin-streptavidin system to position actin and microtubules within the TIRF imaging plane. Other coatings and systems may be used (e.g., antibodies, poly-L-lysine, NEM myosin, etc.).
<ol>
	<li>Thaw aliquots of PEG-silane and biotin-PEG-silane powders.</li>
	<li>Dissolve PEG powders in 80% ethanol (pH 2.0) to generate coating stock solutions of 10 mg/mL mPEG-silane and 2-4 mg/mL biotin-PEG-silane, just before the use. 
	NOTE: PEG powders often appear dissolved but may not be at the microscopic level. Proper resuspension takes ~1-2 min with constant pipetting. Users are encouraged to pipette an additional 10 times following the appearance of powder dissolution. 
	CAUTION: Wear gloves to protect skin from concentrated HCl when making 80% ethanol (pH 2.0).</li>
	<li>Remove the clean (24 mm x 60 mm, #1.5) coverslip from ethanol storage using forceps. Dry with nitrogen gas and store in a clean Petri dish.</li>
	<li>Coat coverslips with 100 &#181;L of coating solution: a mixture of 2 mg/mL mPEG-silane (MW 2,000) and 0.04 mg/mL biotin-PEG-silane (MW 3,400) in 80% ethanol (pH 2.0). 
	NOTE: For sparse coating (recommended) use 2 mg/mL mPEG-silane and 0.04 mg/mL biotin-PEG-silane. For dense coating use 2 mg/mL mPEG-silane, 4 mg/mL biotin-PEG-silane.</li>
	<li>Incubate coverslips at 70 &#176;C for at least 18 h or until use. 
	NOTE: Coated coverslips degrade if stored at 70 &#176;C for more than 2 weeks.</li>
</ol>
3. Assembling imaging flow chambers
<ol>
	<li>Cut 12 strips of double-backed double-sided tape to a length of 24 mm. Remove one side of the tape backing and fix pieces of tape adjacent to the six grooves present on a clean imaging chamber. 
	NOTE: Tape must be flat for proper assembly, otherwise imaging chambers will leak. Carefully remove the tape backing to avoid bumps. Sliding taped chambers on a clean surface to smooth tape-chamber contacts is recommended.</li>
	<li>Remove the second piece of tape backing to expose the sticky side of the tape along each chamber groove. Place chamber tape side up on a clean surface.</li>
	<li>Mix epoxy resin and hardener solutions 1:1 (or according to manufacturer&#39;s instructions) in a small weigh boat.</li>
	<li>Use a P1000 tip to place a drop of mixed epoxy between the tape strips at the end of each imaging chamber groove (red arrow; Figure 1A). Place chamber tape/epoxy side up on a clean surface.</li>
	<li>Remove a coated coverslip from 70 &#176;C incubator. Rinse coated and uncoated surfaces of coverslips with ddH2O six times, dry with filtered nitrogen gas, and then affix to the imaging chamber with the coverslip coating side toward the tape.</li>
	<li>Use a P200 or P1000 pipette tip to apply pressure on the tape-glass interface to ensure a good seal between the tape and the coverslip. 
	NOTE: With a proper seal, double-sided tape becomes translucent. Imaging chambers lacking sufficient tape-chamber contacts will leak.</li>
	<li>Incubate assembled chambers at room temperature for at least 5-10 min to allow the epoxy to fully seal chamber wells before use. Perfusion chambers expire within 12-18 h of assembly. 
	NOTE: Depending on tape placement and the thickness of double-sided tape used, the assembled chamber will have a final volume of 20-50 &#181;L.</li>
</ol>
4. Conditioning of perfusion chambers
<ol>
	<li>Use a perfusion pump (rate set to 500 &#181;L/min) to sequentially exchange conditioning solutions in perfusion chamber as follows:
	<ol>
		<li>Flow 50 &#181;L of 1% BSA to prime the imaging chamber. Remove excess buffer from Luer lock fitting reservoir.</li>
		<li>Flow 50 &#181;L of 0.005 mg/mL streptavidin. Incubate for 1-2 min at room temperature. Remove excess buffer from reservoir.</li>
		<li>Flow 50 &#181;L of 1% BSA to block nonspecific binding. Incubate for 10-30 s. Remove excess buffer from reservoir.</li>
		<li>Flow 50 &#181;L of warm (37 &#176;C) 1x TIRF buffer (1x BRB80, 50 mM KCl, 10 mM DTT, 40 mM glucose, 0.25% (v/v) methylcellulose (4,000 cp)). 
		NOTE: Do not remove excess buffer from the reservoir. This prevents the chamber from drying out, which can introduce air bubbles into the system.</li>
		<li>Optional: Flow 50 &#181;L of stabilized29 and 50% biotinylated microtubule seeds diluted in 1x TIRF buffer. 
		NOTE: The proper dilution must be empirically determined and contain batch to batch variability. Protocols from27,29 are recommended as starting points. A dilution yielding 10-30 seeds per field of view works well with this setup.</li>
	</ol>
	</li>
</ol>
5. Microscope preparation
NOTE: Biochemical reactions containing dynamic actin filaments and microtubules are visualized/performed using an inverted Total Internal Reflection Fluorescence (TIRF) microscope equipped with 120-150 mW solid-state lasers, a temperature corrected 63x oil immersion TIRF objective, and an EMCCD camera. Proteins in this example are visualized at the following wavelengths: 488 nm (microtubules) and 647 nm (actin).
<ol>
	<li>Set the stage/objective heater device to maintain 35-37 &#176;C at least 30 min prior to imaging the first biochemical reaction.</li>
	<li>Set the image acquisition parameters as follows:
	<ol>
		<li>Set acquisition interval to every 5 s for 15-20 min.</li>
		<li>Set 488 and 647 laser exposures to 50-100 ms at 5%-10% power. Set appropriate TIRF angle for microscope. 
		NOTE: Regardless of microscope setup, the simplest way to set the laser power, exposure, and TIRF angle is to make adjustments on images of either polymer alone (see 5.2.2.1 and 5.2.2.2, below). Users are strongly encouraged to use the lowest laser power and exposure settings that still permit detection.
		<ol>
			<li>Adjust the polymerization reaction (Figure 1C) to initiate actin filament assembly and acquire images at 647 nm. Make appropriate adjustments.</li>
			<li>Adjust the polymerization reaction in a second conditioned perfusion well to initiate microtubule assembly (Figure 1C) and visualize at 488 nm. Make appropriate adjustments.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
6. Preparation of protein reaction mixes
<ol>
	<li>Prepare stock solution of fluorescently labelled tubulin.
	<ol>
		<li>Determine the concentration of homemade unlabeled tubulin via spectrophotometry at Abs280, as follows:
		<ol>
			<li>Blank spectrophotometer with 1xBRB80 lacking GTP.</li>
			<li>Calculate the concentration of tubulin using the determined extinction coefficient of 115,000 M-1 cm-1 and the following formula: 
			<img alt="Equation 1" src="/files/ftp_upload/64074/64074eq01.jpg" style="margin: auto;" /></li>
		</ol>
		</li>
		<li>Resuspend commercially-made lyophilized lysine-labeled 488-tubulin to 10 &#181;M (1 mg/mL; 100% label) with 20 &#181;L of 1x BRB80 lacking GTP.</li>
		<li>Thaw a 7.2 &#181;L aliquot of 100 &#181;M unlabeled recycled tubulin29 on ice. 
		NOTE: Recycled tubulin is critical for successful microtubule assembly in vitro because it removes polymerization-incompetent dimers formed in frozen protein stocks29,30.</li>
		<li>Combine 3 &#181;L of 10 &#181;M 488-tubulin with the 7.2 &#181;L aliquot of 100 &#181;M unlabeled tubulin, no more than 15 min before use.</li>
	</ol>
	</li>
	<li>Prepare the stock solution of fluorescently labeled actin.
	<ol>
		<li>For homemade proteins, determine the concentration and percent label of actin via spectrophotometry Abs290 and Abs650, as follows:
		<ol>
			<li>Blank spectrophotometer with G-buffer.</li>
			<li>Calculate the concentration of unlabeled actin using the determined extinction coefficient of 25,974 M-1 cm-1 and the following formula: 
			<img alt="Equation 2" src="/files/ftp_upload/64074/64074eq02.jpg" style="margin: auto;" /></li>
			<li>Calculate the concentration of lysine labeled Alexa-647-actin using the extinction coefficient of unlabeled actin, the fluor correction factor of 0.03, and the following formula: 
			[Alexa-647 actin], &#181;M = (Abs290 -&#160;<img alt="Equation 3" src="/files/ftp_upload/64074/64074eq03.jpg" style="opacity: 0.9; margin: auto;" /></li>
			<li>Calculate the percent label of Alexa-647-actin using the determined &#949; for Alexa-647 of 239,000 M-1 cm-1, as follows: 
			% label of Alexa-647-actin = (Abs290 - (<img alt="Equation 4" src="/files/ftp_upload/64074/64074eq04.jpg" style="margin: auto;" /></li>
		</ol>
		</li>
		<li>Thaw one 2 &#181;L aliquot of 3 &#181;M 100% labeled biotin-actin (labeled on lysine residues). Dilute 10-fold by adding 18 &#181;L of G-buffer.</li>
		<li>Combine 3 &#181;L of diluted biotinylated actin, appropriate volumes of unlabeled and labeled actin (above) such that the final mix will be 12.5 &#181;M total actin with 10%-30% fluorescent label. 
		NOTE: Greater than 30% percent fluorescent actin monomers (final) can compromise imaging resolution as filaments become difficult to discern from the background.</li>
	</ol>
	</li>
	<li>Prepare reaction mixes (Figure 1C).
	<ol>
		<li>Prepare cytoskeleton mix (Tube A) by combining 2 &#181;L of the 12.5 &#181;M actin mix stock (6.2.3) with the tubulin stock mix (6.1.4), no more than 15 min prior to imaging. Store on ice until use.</li>
		<li>Prepare protein reaction mix (Tube B) by combining all other experimental components and proteins, including: 2x TIRF buffer, anti-bleach, nucleotides, buffers, and accessory proteins. An example is shown in Figure 1C. 
		NOTE: The final dilution results in a 1x TIRF buffer that contains ATP, GTP, and ionic strength within the estimated physiological range.</li>
	</ol>
	</li>
	<li>Incubate Tube A and Tube B separately at 37 &#176;C for 30-60 s. To initiate reaction, mix and add the contents of Tube B to Tube A (below).</li>
</ol>
7. Image actin and microtubule dynamics
<ol>
	<li>Condition perfusion well (Figure 1B; step 4, above).</li>
	<li>Initiate actin and microtubule assembly simultaneously by adding the contents of Tube B (reaction mix) to Tube A (cytoskeleton mix) (Figure 1C).</li>
	<li>Flow 50 &#181;L of reaction containing 1x TIRF buffer supplemented with 15 &#181;M free tubulin, 1 mM GTP, and 0.5 &#181;M actin monomers and appropriate volumes of buffer controls.</li>
	<li>Record time-lapse movie using microscope software to acquire every 5 s for 15-20 min. 
	NOTE: Initiation of actin and microtubule dynamics occurs within 2-5 min (Figure 2). Longer delays indicate problems with temperature control or concentration-related problems of proteins in the reaction mix.</li>
	<li>Condition a new perfusion well (step 4) and replace buffer volume with regulatory protein(s) of interest (i.e., Tau) and buffer controls (Figure 1C). Acquire as outlined in step 7 (above) to assess regulatory proteins for emergent actin-microtubule functions.</li>
</ol>
8. Process and analyze images using FIJI software31
<ol>
	<li>Open saved TIRF movies and view as a composite.</li>
	<li>Analyze microtubule dynamics (Figure 3A), as follows:
	<ol>
		<li>Generate a time-based maximum Z-projection from the image stacks menu.</li>
		<li>Synchronize Z-projection window with the original TIRF movie from the Analyze&#62; Tools&#62; Synchronize Windows menu.</li>
		<li>Draw a line using the straight-line tool along a microtubule of interest on the time projected image.
		<ol>
			<li>Open the region of interest (ROI) manager from the analyze menu (Analyze&#62; Tools&#62; ROI Manager).</li>
			<li>Save individual microtubule locations by pressing &#34;t&#34;. Repeat for all microtubules of interest.</li>
		</ol>
		</li>
		<li>Plot kymographs of selected lines using &#34;/&#34; or run the multi-kymo macro that generates a video and kymograph for every microtubule in the ROI manager31.
		<ol>
			<li>Add both length (&#181;m) and time (min) scale bars to kymographs from the Analyze&#62; Tools&#62; Scale bars menu.</li>
		</ol>
		</li>
		<li>Measure microtubule growth speeds from kymograph slopes (Figure 3A, 1-2; slope of black lines).</li>
		<li>Count dynamic microtubule events (catastrophe or regrowth) from the generated kymograph or using available analysis macros5,8,18,25. Red dotted lines in Figure 3A, 1-2 represent catastrophe/rapid disassembly events.</li>
	</ol>
	</li>
	<li>Analyze actin dynamics (Figure 3B), as follows:
	<ol>
		<li>Measure actin nucleation, as follows:
		<ol>
			<li>Count the number of actin filaments present in the field of view 100 s after the initiation of the reaction and express by the area (filaments per &#181;m2).</li>
			<li>Record and save data in ROI manager, as in step 8.2.3.1, above.</li>
		</ol>
		</li>
		<li>Measure actin filament elongation rates (Figure 3B), as follows:
		<ol>
			<li>Draw a line along an actin filament of interest using the segmented-line tool.</li>
			<li>Add line to ROI manager as in step 8.2.3.1, above.</li>
			<li>Repeat following the line (adding each measurement to ROI manager) for at least four movie frames. 
			NOTE: Measuring seven to eight consecutive frames is recommended, however some conditions slow actin polymerization below the detectable limit that can be resolved by objective/microscope setups. In such a case, measurements can be made at regular intervals over non-consecutive frames, (e.g., every five frames).</li>
			<li>Plot measured length values over elapsed time. The slope of the generated line is the actin elongation rate in microns/s.</li>
			<li>Convey final calculated rates as subunits s-1 &#181;M-1 using a correction factor of 370 subunits to account for the number of actin monomers in a micron of filament32.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Perform correlative analysis for regions of parallel actin-microtubule association (Figure 3C), as follows:
	<ol>
		<li>Draw a line along a microtubule of interest at a specific time point (i.e., 300 s after reaction initiation), using the straight-line tool.
		<ol>
			<li>Add line to ROI manager as in step 8.2.3.1, above.</li>
		</ol>
		</li>
		<li>Plot the fluorescence intensity along the line in each channel.
		<ol>
			<li>Select each channel with the image slider and plot the intensities along the line using &#34;command k&#34;.</li>
			<li>Save or export values by clicking the &#34;list&#34; button in the output window.</li>
		</ol>
		</li>
		<li>Express actin-microtubule coupling events as a ratio (actin overlapping with microtubules) from individual events or as a count of events in a given field of view at a consistent timepoint (Figure 3C).</li>
		<li>Alternative: Use software to determine the percent overlap of both channels5,12.</li>
	</ol>
	</li>
</ol>

There are no conflicts of interest to disclose.

The use of total internal reflection fluorescence (TIRF) microscopy to visualized purified proteins has been a fruitful and compelling approach to dissect unique mechanisms of cytoskeletal regulation5,23,24,25,26,27,35. Compared to traditional biochemical assays, TIRF reactions require very small volumes (50-100 &#181;L), and quantitative measurements of cytoskeletal dynamics can be gleaned from an individual assay. Most studies of cytoskeletal dynamics focus on a single polymer system (i.e., actin filaments or microtubules), thus detailed measurements of the crosstalk or emergent behaviors between actin filaments and microtubules typically seen in cells have remained elusive and difficult to recapitulate in the test tube. To solve this problem, this protocol describes a single-filament TIRF microscopy system that enables the direct visualization of dynamic actin and microtubule polymers in the same biochemical reaction. Thus, this method goes beyond traditional assays that recapitulate the dynamic behavior of actin filaments or microtubules alone. This technique was also performed with Tau as an example of how several dynamic properties change in the presence of a cytoskeleton coupling factor. This protocol can be used with additional proteins known or suspected to coordinate actin or microtubule dynamics, including (but not limited to) MACF, GAS, formins, and more. Finally, provided example analyses can be used as a guide to quantify data acquired with this protocol.
&#34;Seeing is believing&#34; is a compelling reason to perform microscopy-based assays. However, caution is required in the execution and interpretation of TIRF microscopy experiments. One major challenge of cytoskeletal co-assembly assays is that many commonly used imaging conditions are not compatible each polymer. Microtubules and actin typically have different buffer, temperature, salt, nucleotide, and concentration requirements for polymerization. Actin, tubulin, regulatory proteins of interest, and the buffers utilized in this protocol are sensitive to freeze-thaw cycles. Therefore, careful handling of proteins and buffers is necessary to successfully execute this protocol. To alleviate many of these concerns, using freshly recycled tubulin (frozen for &#60;6 weeks), and pre-clearing frozen/resuspended actins via ultracentrifugation is strongly recommended. These considerations also apply to the myriad of regulatory proteins to be assessed with this procedure, which may be sensitive to freeze-thaw cycles or the concentration of buffer salts5,11,36.
Unfortunately, no one-size-fits-all buffer without experimental tradeoffs exists. To appropriate more volume for proteins of lower concentration, ATP and GTP may be included in the 2x TIRF buffer solution (Figure 1C). However, because these nucleotides are extremely sensitive to freeze-thaw cycles, it is not recommended. The oxygen scavenging compounds used here (i.e., catalase and glucose-oxidase) are necessary to visualize proteins for long periods of time (minutes to hours), but are known to restrict microtubule polymerization at high concentrations5. Related to these buffer considerations, a limitation of this protocol is that some canonical microtubule-associated regulatory proteins may require more or less salt to recapitulate functions found in cells or assays using microtubules alone (without actin). Changing the nature or concentration of salt to address these concerns will likely influence rates of actin filament polymerization and/or parameters of microtubule dynamics. Measurements of multiple descriptive parameters (minimally, nucleation, elongation rates, and stability) (Figure 3) are required to confirm protocol success or to explicitly document the effects of specific buffers or regulatory proteins. For example, too much actin filament polymerization can obscure actin-microtubule coupling events within seconds. Consequently, fine-tuning experimental conditions by lowering the overall concentration of actin or including additional proteins to suppress actin nucleation (i.e., profilin) will extend the overall period that coordinated actin-microtubule activities can be viewed clearly. Controls addressing these prerequisites, and technical replicates (beyond multiple fields of view), are critical for users to generate reliable and reproducible results.
Cell-based studies provide limited opportunity to observe direct protein-protein relationships or the action of regulatory complexes. In contrast, some of the mechanisms gleaned from in vitro assays do not always reflect the exact behaviors of proteins seen in cells. This classic biochemist dilemma can be addressed in future applications of this technique with specific modifications. For example, adding functional fluorescently labeled coupling proteins expands this method from single-filament studies to single-molecule studies. Assays can be further modified to use cell extracts that may add the &#34;missing&#34; unknown key factors required to recapitulate cell-like phenomena. For example, TIRF-based assays employing yeast or Xenopus extracts have reconstituted contractile actomyosin rings37, mitotic spindles26,38, components of actin or microtubule assembly39,40, and even dynamics at the centrosome and kinetochores36,41,42,43. Moreover, such systems may pave the way toward artificial cell systems that have lipids or signaling factors present44,45,46.

Historically, actin and microtubules have been viewed as separate entities, each with their own set of regulatory proteins, dynamics behaviors, and distinct cellular locations. Abundant evidence now demonstrates that actin and microtubule polymers engage in functional crosstalk mechanisms that are essential to execute numerous cell processes including migration, mitotic spindle positioning, intracellular transport, and cell morphology1,2,3,4. The diverse coordinated behaviors that underlie these examples are dependent on an intricate balance of coupling factors, signals, and physical properties. However, the molecular details that underpin these mechanisms are still largely unknown because most studies focus on a single cytoskeletal polymer at a time1,2,5.
Actin and microtubules do not directly interact6,7,8. The coordinated dynamics of actin and microtubules seen in cells is mediated by additional factors. Many proteins thought to regulate actin-microtubule crosstalk have been identified and their activities are well characterized with regard to either cytoskeletal polymer alone1,2. Growing evidence suggests this single polymer approach has concealed the dual functions of some of the proteins/complexes that enable actin-microtubule coupling events7,8,9,10,11,12,13. Experiments where both polymers are present are rare and often define mechanisms with a single dynamic polymer and static stabilized version of the other6,8,9,10,11,14,15,16,17,18. Thus, methods are needed to investigate the emergent properties of actin-microtubule coordinating proteins that may only be fully understood in experimental systems that employ both dynamic polymers.
The combination of direct protein labeling approaches, genetically encoded affinity tags, and total internal reflection fluorescence (TIRF) microscopy has been applied with great success in biomimetic reconstitution systems19,20,21,22,23. Many bottom-up schemes do not contain all the factors that regulate proteins in cells. However, &#34;biochemistry on a coverglass&#34; technology has refined many mechanisms of actin and microtubule dynamics at high spatial and temporal scales, including the components required for polymer assembly or disassembly, and motor protein movement5,12,23,24,25,26,27. Here a minimal component single-filament approach to investigate actin-microtubule coupling in vitro is described. This protocol can be used with commercially available or highly pure purified proteins, fluorescently labeled proteins, perfusion chambers, and extended to more complicated schemes containing cell extracts or synthetic systems. Here, commercially available Tau protein is used to demonstrate how cytoskeletal dynamics change in the presence of an actin-microtubule coupling protein, but can be substituted for other putative actin-microtubule coordinating factors. The major advantage of this system over other approaches is the ability to simultaneously monitor the dynamics of multiple cytoskeletal polymers in one reaction. This protocol also provides users with examples and simple tools to quantify changes to cytoskeletal polymers. Thus, protocol users will produce reliable, quantitative, single-filament resolution data to describe mechanisms that underlie how diverse regulatory proteins coordinate actin-microtubule dynamics.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1% BSA (w/v)</td>
			<td>Fisher Scientific</td>
			<td>BP1600-100</td>
			<td>For this purpose (blocking TIRF chambers), BSA is resuspended in ddH20 and filtered through a 0.22 &#181;m filter.</td>
		</tr>
		<tr>
			<td>1&#215; BRB80</td>
			<td>Homemade</td>
			<td></td>
			<td>80 mM PIPES, 1 mM MgCl2, 1 mM EGTA, pH 6.8 with KOH</td>
		</tr>
		<tr>
			<td>10 mg/mL (1000 U) glucose oxidase</td>
			<td>Sigma Aldrich Inc, St. Louis, MO</td>
			<td>G2133-50KU</td>
			<td>Combined with catalase, aliquot and store at -80 oC until use</td>
		</tr>
		<tr>
			<td>100 &#181;M tubulin</td>
			<td>Cytoskeleton Inc, Denver, CO</td>
			<td>T240</td>
			<td>Homemade tubulins should be recycled before use to remove polymerization-incompetent tubulin (Hyman et al. (1992)29; Li and Moore (2020)30). Commercially available tubulins are often too dilute to recycle, but function well if resuspended according to manufacturer&#8217;s instructions and pre-cleared via ultracentrifugation (278,000 &#215; g) for 60 min, before use.</td>
		</tr>
		<tr>
			<td>100 mM ATP</td>
			<td>Gold Biotechnology Inc, Olivette, MO</td>
			<td>A-081</td>
			<td>Resuspended in ddH20 (pH 7.5) and filter sterilized.</td>
		</tr>
		<tr>
			<td>100 mM GTP</td>
			<td>Fisher Scientific</td>
			<td>AC226250010</td>
			<td>Resuspended in 1&#215; BRB80 (pH 6.8) and filter sterilized.</td>
		</tr>
		<tr>
			<td>120-150 mW solid-state lasers</td>
			<td>Leica Microsystems</td>
			<td>11889151; 11889148</td>
			<td></td>
		</tr>
		<tr>
			<td>2 mg/mL catalase</td>
			<td>Sigma Aldrich Inc, St. Louis, MO</td>
			<td>C40-100</td>
			<td>Combined with glucose oxidase, aliquot and store at -80 oC until use</td>
		</tr>
		<tr>
			<td>2&#215; TIRF buffer</td>
			<td>Homemade</td>
			<td></td>
			<td>2&#215; BRB80, 100 mM KCl, 20 mM DTT, 80 mM glucose, 0.5% (v/v) methylcellulose (4,000 cp); Note: 1 &#181;L of 0.1M GTP and 1 &#181;L of 0.1M ATP added separately to TIRF reactions to avoid repeated freeze-thaw cycles.</td>
		</tr>
		<tr>
			<td>24 &#215; 60 mm, #1.5 coverglass</td>
			<td>Fisher Scientific, Waltham, MA</td>
			<td>22-266882</td>
			<td>Coverglass must be extensively washed before use (Smith et al. (2014)22)</td>
		</tr>
		<tr>
			<td>37 oC heatblock</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>37 oC water bath</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>5 mg/mL Streptavidin (600x stock)</td>
			<td>Avantor, Philadelphia, PA</td>
			<td>RLS000-01</td>
			<td>Resuspended in Tris-HCl (pH 8.8); dilute the aliquot to 1&#215; in HEK buffer on day of use</td>
		</tr>
		<tr>
			<td>5 min Epoxy resin and hardener</td>
			<td>Loctite, Rocky Hill, CT</td>
			<td>1365736</td>
			<td>Combined resin and hardener may take up to 30 min to cure.</td>
		</tr>
		<tr>
			<td>50% biotinylated-GpCpp microtubule seeds</td>
			<td>Cytoskeleton Inc; Homemade</td>
			<td>T333P</td>
			<td>(optional) GppCpp or Taxol stabilized microtubule seeds can more efficiently mediate microtubule polymerization. Taxol and GppCpp stabilize microtubules in different ways that can affect the microtubule lattice structure and ability of certain regulatory proteins to bind to the stabilized portion of the microtubule. A method to make diverse kinds of microtubule seeds is outlined in Hyman et al. (1992).</td>
		</tr>
		<tr>
			<td>70 oC incubator</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Actin mix stock</td>
			<td>Homemade; this protocol</td>
			<td></td>
			<td>A 12.5 &#181;M actin mix comprised of labeled (fluorescent and biotinylated) and unlabeled actin for up to six reactions. 2 &#181;L of stock is used in the final TIRF reaction. The final concentration of actin used in each reaction is 0.5 &#181;M (10% Alexa-647; 0.09% biotin-labeled).</td>
		</tr>
		<tr>
			<td>Appropriate buffer controls</td>
			<td>Homemade</td>
			<td></td>
			<td>Combination of buffers from all proteins being assessed</td>
		</tr>
		<tr>
			<td>Biotin-PEG-silane (MW 3,400)</td>
			<td>Laysan Bio Inc</td>
			<td>biotin-PEG-SIL-3400</td>
			<td>Dispensed into 2-5 mg aliquots, backfilled with nitrogen, parafilmed closed, and stored at -20 oC with desiccant until use</td>
		</tr>
		<tr>
			<td>Biotinylated actin</td>
			<td>Cytoskeleton Inc; Homemade</td>
			<td>AB07</td>
			<td>Biotin-actin is made by labeling on lysine residues and thus assumed to be at least 100% labeled, but varies with different lots/preparations.&#160; Optimal biotinylated actin concentrations must be empirically determined for particular uses/experimental designs. Higher concentrations permit more efficient tracking, but may impede polymerization or interactions with regulatory proteins. Here a small percentage (0.09% or 900 pM) biotinylated actin is present in the final TIRF reaction.</td>
		</tr>
		<tr>
			<td>Dishsoap</td>
			<td>Dawn, Procter and Gamble, Cincinnati, OH</td>
			<td></td>
			<td>For unknown reasons, the blue version cleans coverslips more efficiently than other available colors.</td>
		</tr>
		<tr>
			<td>Dry ice</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FIJI Software</td>
			<td>www.https://imagej.net/software/fiji/downloads</td>
			<td></td>
			<td>Schneider et al. (2012)31.</td>
		</tr>
		<tr>
			<td>Fluorescently labeled actin</td>
			<td>Cytoskeleton Inc; Homemade</td>
			<td>AR05</td>
			<td>Homemade fluorescently labeled actin is stored in G-buffer supplemented with 50% glycerol at -20 oC (Spudich et al. (1971)47; Liu et al. (2022)48). Fluorescently labeled actin is dialyzed against G-buffer and precleared via ultracentrifugation for 60 min at 278,000 &#215; g before use.</td>
		</tr>
		<tr>
			<td>Fluorescently labeled tubulin</td>
			<td>Cytoskeleton Inc</td>
			<td>TL488M, TLA590M, TL670M</td>
			<td>Resuspended in 20 &#181;L 1&#215; BRB80 (10 &#181;M final concentration) and pre-cleared via ultracentrifugation (278,000 &#215; g) for 60 min, before use.</td>
		</tr>
		<tr>
			<td>G-buffer</td>
			<td>Homemade</td>
			<td></td>
			<td>3 mM Tris-HCl (pH 8.0), 0.2 mM CaCl2, 0.5 mM DTT, 0.2 mM ATP</td>
		</tr>
		<tr>
			<td>HEK Buffer</td>
			<td>Homemade</td>
			<td></td>
			<td>20 mM HEPES (pH 7.5), 1 mM EDTA (pH 8.0), 50 mM KCl</td>
		</tr>
		<tr>
			<td>Ice</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Ice bucket</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Imaging chambers</td>
			<td>IBIDI, Fitchburg, WI</td>
			<td>80666</td>
			<td>Order chambers with no bottom to utilize different coverslip coatings</td>
		</tr>
		<tr>
			<td>iXon Life 897 EMCCD camera</td>
			<td>Andor, Belfast, Northern Ireland</td>
			<td>8114137</td>
			<td></td>
		</tr>
		<tr>
			<td>LASX Premium microscope software</td>
			<td>Leica Microsystems</td>
			<td>11640611</td>
			<td></td>
		</tr>
		<tr>
			<td>Methylcellulose (4,000 cp)</td>
			<td>Sigma Aldrich Inc</td>
			<td>M0512</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope base equipped with TIRF module</td>
			<td>Leica Microsystems, Wetzlar, Germany</td>
			<td>11889146</td>
			<td></td>
		</tr>
		<tr>
			<td>mPEG-silane (MW 2,000)</td>
			<td>Laysan Bio Inc, Arab, AL</td>
			<td>mPEG-SIL-2000</td>
			<td>Dispensed into 10-15 mg aliquots, backfilled with nitrogen, parafilmed closed, and stored at -20 oC with desiccant until use</td>
		</tr>
		<tr>
			<td>Objective heater and heated stage insert</td>
			<td>OKO labs, Pozzioli, Italy</td>
			<td>8113569</td>
			<td>Set temperature controls to 35-37 oC. Use manufacturer suggestions for accurate calibration.</td>
		</tr>
		<tr>
			<td>Perfusion pump</td>
			<td>Harvard Apparatus, Holliston, MA</td>
			<td>704504</td>
			<td>A syringe and tubing can be substituted.</td>
		</tr>
		<tr>
			<td>Petri Dish, 100 x 15 mm</td>
			<td>Genesee Scientific, San Diego, CA</td>
			<td>32-107</td>
			<td></td>
		</tr>
		<tr>
			<td>Plastic slide mailer container</td>
			<td>Fisher Scientific</td>
			<td>HS15986</td>
			<td></td>
		</tr>
		<tr>
			<td>SA-S-1L-SecureSeal 0.12 mm thick</td>
			<td>Grace Biolabs, Bend, OR</td>
			<td>620001</td>
			<td>Double-sided tape of precise manufactured dimensions is strongly recommended.</td>
		</tr>
		<tr>
			<td>Small styrofoam container</td>
			<td>Abcam, Cambridge, UK</td>
			<td></td>
			<td>Reused from shipping</td>
		</tr>
		<tr>
			<td>Small weigh boat</td>
			<td>Fisher Scientific</td>
			<td>02-202-100</td>
			<td></td>
		</tr>
		<tr>
			<td>Spectrophotometer</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Tau</td>
			<td>Cytoskeleton Inc</td>
			<td>TA01</td>
			<td>Three isoforms of Tau are present in the commercially available preparation of Tau. The concentration in this protocol was determined from the highest molecular weight band (14.3 &#181;M, when resuspended per manufacturer&#8217;s recommendations with 50 &#181;L of ddH20).</td>
		</tr>
		<tr>
			<td>Temperature corrected 63&#215; Plan Apo 1.47 N.A. oil immersion TIRF objective</td>
			<td>Leica Microsystems</td>
			<td>11506319</td>
			<td></td>
		</tr>
		<tr>
			<td>Tubulin stock</td>
			<td>Homemade; this protocol</td>
			<td></td>
			<td>A tubulin stock consisting of 7.2 &#181;L recycled 100 &#181;M unlabeled tubulin and 3 &#181;L of 10 &#181;M resuspended commercially available fluorescently labeled tubulin. One tubulin stock is used per reaction and thawed/stored on ice. The final concentration of free tubulin in each reaction is 15 &#181;M (4% labeled). More than 15 &#181;M tubulin will result in hyperstabilized (not dynamic) microtubules, whereas concentrations below 7.5 &#181;M free tubulin do not polymerize well. Careful determination of protein concentration and handling is required.</td>
		</tr>
		<tr>
			<td>Unlabeled actin (dark)</td>
			<td>Cytoskeleton Inc; Homemade</td>
			<td>AKL99</td>
			<td>Actin nucleates are almost always present in commercially available (lyophilized) or frozen actins and contribute to variability in quantitative measurements (Spudich et al. (1971)47; Liu et al. (2022)48). Rabbit muscle actin is stored in G-buffer at -80 oC and precleared via ultracentrifugation for 60 min at 278,000 &#215; g before use.&#160;Several actin stock solutions are made throughout the day (making no more than enough for six reactions at a time&#160;is strongly recommended).</td>
		</tr>
	</tbody>
</table>

visualizing actin and microtubule coupling dynamics in vitro by total internal reflection fluorescence (tirf) microscopy

Traditionally, the actin and microtubule cytoskeletons have been studied as separate entities, restricted to specific cellular regions or processes, and regulated by different suites of binding proteins unique for each polymer. Many studies now demonstrate that the dynamics of both cytoskeletal polymers are intertwined and that this crosstalk is required for most cellular behaviors. A number of proteins involved in actin-microtubule interactions have already been identified (i.e., Tau, MACF, GAS, formins, and more) and are well characterized with regard to either actin or microtubules alone. However, relatively few studies showed assays of actin-microtubule coordination with dynamic versions of both polymers. This may occlude emergent linking mechanisms between actin and microtubules. Here, a total internal reflection fluorescence (TIRF) microscopy-based in vitro reconstitution technique permits the visualization of both actin and microtubule dynamics from the one biochemical reaction. This technique preserves the polymerization dynamics of either actin filament or microtubules individually or in the presence of the other polymer. Commercially available Tau protein is used to demonstrate how actin-microtubule behaviors change in the presence of a classic cytoskeletal crosslinking protein. This method can provide reliable functional and mechanistic insights into how individual regulatory proteins coordinate actin-microtubule dynamics at a resolution of single filaments or higher-order complexes.

With the conditions described above (Figure 1), actin and microtubule polymers should be visible (and dynamic) within 2 min of image acquisition (Figure 2). As with any biochemistry-based protocol, optimization may be required for different regulatory proteins or batches of protein. For these reasons, the TIRF angle and image exposures are set first with reactions containing each individual polymer. This confirms that stored proteins are functional and enough labeled protein is present for detection. While not always necessary (and not performed here), post-processing of movies (i.e., background subtraction, averaging, or Fourier transformations) can be used to enhance the image contrast (particularly of microtubules)5,25,33. The direct visualization of single actin filaments and microtubules afforded by this assay supports the quantitative determination of several dynamic measures for either cytoskeleton component alone or together, including polymerization parameters (i.e., nucleation or elongation rate), disassembly parameters (i.e., shrinkage rates or catastrophe events), and polymer coalignment/overlap (Figure 3). Further, these measures can be used as a starting point to decipher the binding or influence of regulatory ligands like Tau (Figure 3). Many measurements of single actin filaments or microtubules can be made from one TIRF movie. However, due to variations in coverslip coating, pipetting, and other factors, reliable measurements should also include multiple technical replicate reactions/movies.
Many facets of microtubule dynamics can be determined from example kymographs including the rate of microtubule elongation, as well as the frequency of catastrophe and rescue events (Figure 3A). Using kymographs to measure actin dynamics in this system is not as straightforward because actin filaments are more convoluted than microtubules. As a consequence, parameters of actin filament dynamics are measured by hand, which is time consuming and labor intensive. Nucleation counts are measured as the number of actin filaments present at a consistent timepoint for all conditions. These counts vary widely across TIRF imaging fields, but can be used with many replicates or to supplement observations from other polymerization assays. Nucleation counts may also be used for microtubules if trial conditions lack stabilized microtubule seeds. Actin filament elongation rates are measured as the length of filament over time from at least four movie frames. Rate values are conveyed per micromolar actin with a correction factor of 370 subunits to account for the number of actin monomers in a micron of filament (Figure 3B)32. Measurements to define the coordinated behaviors between actin and microtubules are less well defined. However, correlative analyses have been applied to measure the coincidence of both polymers including line scans (Figure 3C) or overlap software5,11,34.
Data Availability: 
All datasets associated with this work have been deposited in Zenodo and are available with reasonable request at: 10.5281/zenodo.6368327.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/64074/64074fig01.jpg" /> 
Figure 1. Experimental schematics: flow chamber assembly to image acquisition.&#160;(A) Imaging chamber assembly. Top to bottom: IBIDI imaging chambers are taped along perfusion wells (denoted by arrow); the second (white) layer of tape backing (left on in the image shown to better orient users) is removed and Epoxy is applied at the edge of the perfusion chamber (arrow). Note: To more easily orient users where to place the epoxy, the white backing was left on in this image. The cleaned and coated coverslip is attached to the imaging chamber with the coating side facing the inside of the perfusion well. (B) Flow-chart illustrating the steps for conditioning imaging chambers for biotin-streptavidin linkages. (C) Examples of reactions used to acquire TIRF movies of dynamic microtubules and actin filaments. <a href="https://www.jove.com/files/ftp_upload/64074/64074fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/64074/64074fig02.jpg" /> 
Figure 2. Image sequences of growing actin filaments and microtubules in the absence or presence of Tau. Time-lapse image montage from TIRF assays containing 0.5 &#181;M actin (10% Alexa-647-actin and 0.09% biotin-actin labeled) and 15 &#181;M free tubulin (4% HiLyte-488 labeled) in the absence (A) or presence (B) of 250 nM Tau. Time elapsed from reaction initiation (mixing Tube A and Tube B) is shown. Scale bars, 25 &#181;m. <a href="https://www.jove.com/files/ftp_upload/64074/64074fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/64074/64074fig03.jpg" /> 
Figure 3. Example measurements of microtubules and actin filament dynamics. (A) Average time projection of the tubulin channel efficiently visualizes total microtubule lengths for the line scans used to generate kymograph plots. Black dotted lines correspond to the two example kymographs of dynamic microtubules shown on the right. The growth (solid black lines) and disassembly phases (doted pink lines; two denoted with pink arrows) of microtubules are shown on each kymograph. Time scale bar, 3 min. Length scale bar, 10 &#181;m. Reaction contains 0.5 &#181;M actin (10% 647-label) and 15 &#181;M free tubulin (4% 488-HiLyte label). Only the tubulin channel is shown.(B) Two example time-lapse image montages depicting single-actin filaments actively polymerizing. Elongation rates are calculated as the slope of plots of the length of actin filaments over time per micromolar actin. Thus, a correction factor of two must be applied to 0.5 &#181;M actin reactions for comparison for rates typically determined at the 1 &#181;M actin concentration. Examples from five filaments are shown to the right. Scale bars, 10 &#181;m. Reaction contains 0.5 &#181;M actin (10% 647-label) and 15 &#181;M free tubulin (4% 488-HiLyte label). Only the actin channel is shown. (C) TIRF images of dynamic microtubules (MT) (green) and actin filaments (purple) polymerizing in the absence (left) or presence of 250 nM Tau (middle). Blue dotted lines and arrows mark where a line was drawn for the line scan plots corresponding to each condition (below each image). Overlap between microtubules and actin regions (shown as black) can be scored at a set time point per area (right). Scale bars, 25 &#181;m. Reactions contain 0.5 &#181;M actin (10% 647-label) and 15 &#181;M free tubulin (4% 488-HiLyte label) with or without 250 nM Tau. <a href="https://www.jove.com/files/ftp_upload/64074/64074fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy at JoVE.com

Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy

This protocol is a guide for visualizing dynamic actin and microtubules using an in vitro total internal fluorescence (TIRF) microscopy assay.

Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy

Traditionally, the actin and microtubule cytoskeletons have been studied as separate entities, restricted to specific cellular regions or processes, and ...

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Research

JoVE Journal

Biochemistry

3.3K Views.  State University of New York (SUNY) Upstate Medical University. This protocol is a guide for visualizing dynamic actin and microtubules using an in vitro total internal fluorescence (TIRF) microscopy assay. 

Video: Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy

In Vitro Polymerization of F-actin on Early Endosomes

Many early endosome functions, particularly cargo protein sorting and membrane deformation, depend on patches of short F-actin filaments nucleated onto the endosomal membrane. We have established a microscopy-based in vitro assay that reconstitutes the nucleation and polymerization of F-actin on early endosomal membranes in test tubes, thus rendering this complex series of reactions amenable to genetic and biochemical manipulations. Endosomal fractions are prepared by floatation in sucrose gradients from cells expressing the early endosomal protein GFP-RAB5. Cytosolic fractions are prepared from separate batches of cells. Both endosomal and cytosolic fractions can be stored frozen in liquid nitrogen, if needed. In the assay, the endosomal and cytosolic fractions are mixed, and the mixture is incubated at 37 &#176;C under appropriate conditions (e.g., ionic strength, reducing environment). At the desired time, the reaction mixture is fixed, and the F-actin is revealed with phalloidin. Actin nucleation and polymerization are then analyzed by fluorescence microscopy. Here, we report that this assay can be used to investigate the role of factors that are involved either in actin nucleation on the membrane, or in the subsequent elongation, branching, or crosslinking of F-actin filaments.

In Vitro Polymerization of F-actin on Early Endosomes

Early endosome functions depend on F-actin polymerization. Here, we describe a microscopy-based in vitro assay that reconstitutes the nucleation and polymerization of F-actin on early endosomal membranes in test tubes, thus rendering this complex series of reactions amenable to biochemical and genetic manipulations.

Many early endosome functions, particularly cargo protein sorting and membrane deformation, depend on patches of short F-actin filaments nucleated onto ...

Using In Vitro Fluorescence Resonance Energy Transfer to Study the Dynamics Of Protein Complexes at a Millisecond Time Scale

Proteins are the primary operators of biological systems, and they usually interact with other macro- or small molecules to carry out their biological functions. Such interactions can be highly dynamic, meaning the interacting subunits are constantly associated and dissociated at certain rates. While measuring the binding affinity using techniques such as quantitative pull-down reveals the strength of the interaction, studying the binding kinetics provides insights on how fast the interaction occurs and how long each complex can exist. Furthermore, measuring the kinetics of an interaction in the presence of an additional factor, such as a protein exchange factor or a drug, helps reveal the mechanism by which the interaction is regulated by the other factor, providing important knowledge for the advancement of biological and medical research. Here, we describe a protocol for measuring the binding kinetics of a protein complex that has a high intrinsic association rate and can be dissociated quickly by another protein. The method uses fluorescence resonance energy transfer to report the formation of the protein complex in vitro, and it enables monitoring the fast association and dissociation of the complex in real time on a stopped-flow fluorimeter. Using this assay, the association and dissociation rate constants of the protein complex are quantified.

Protein-protein interactions are critical for biological systems, and studies of the binding kinetics provide insights into the dynamics and function of protein complexes. We describe a method that quantifies the kinetic parameters of a protein complex using fluorescence resonance energy transfer and the stopped-flow technique. &#160;

Proteins are the primary operators of biological systems, and they usually interact with other macro- or small molecules to carry out their biological ...

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

The signaling and function of a cell are dictated by the dynamic structures and interactions of its surface receptors. To truly understand the structure-function relationship of these receptors in situ, we need to visualize and track them on the live cell surface with enough spatiotemporal resolution. Here we show how to use recently developed Lattice Light-Sheet Microscopy (LLSM) to image T-cell receptors (TCRs) four-dimensionally (4D, space and time) at the live cell membrane. T cells are one of the main effector cells of the adaptive immune system, and here we used T cells as an example to show that the signaling and function of these cells are driven by the dynamics and interactions of the TCRs. LLSM allows for 4D imaging with unprecedented spatiotemporal resolution. This microscopy technique therefore can be generally applied to a wide array of surface or intracellular molecules of different cells in biology.

The goal of this protocol is to show how to use Lattice Light-Sheet Microscopy to four-dimensionally visualize surface receptor dynamics in live cells. Here T cell receptors on CD4+ primary T cells are shown.

The signaling and function of a cell are dictated by the dynamic structures and interactions of its surface receptors. To truly understand the ...

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip

Total internal reflection fluorescence (TIRF) is commonly used in single molecule localization based super-resolution microscopy as it gives enhanced contrast due to optical sectioning. The conventional approach is to use high numerical aperture microscope TIRF objectives for both excitation and collection, severely limiting the field of view and throughput. We present a novel approach to generating TIRF excitation for imaging with optical waveguides, called chip-based nanoscopy. The aim of this protocol is to demonstrate how chip-based imaging is performed in an already built setup. The main advantage of chip-based nanoscopy is that the excitation and collection pathways are decoupled. Imaging can then be done with a low magnification lens, resulting in large field of view TIRF images, at the price of a small reduction in resolution. Liver sinusoidal endothelial cells (LSECs) were imaged using direct stochastic optical reconstruction microscopy (dSTORM), showing a resolution comparable to traditional super-resolution microscopes. In addition, we demonstrate the high-throughput capabilities by imaging a 500 &#181;m x 500 &#181;m region with a low magnification lens, providing a resolution of 76 nm. Through its compact character, chip-based imaging can be retrofitted into most common microscopes and can be combined with other on-chip optical techniques, such as on-chip sensing, spectroscopy, optical trapping, etc. The technique is thus ideally suited for high throughput 2D super-resolution imaging, but also offers great opportunities for multi-modal analysis.

Chip-based super-resolution optical microscopy is a novel approach to fluorescence microscopy and offers advantages in cost effectiveness and throughput. Here, the protocols for chip preparation and imaging are shown for TIRF microscopy and localization-based super-resolution microscopy.

Total internal reflection fluorescence (TIRF) is commonly used in single molecule localization based super-resolution microscopy as it gives enhanced ...

Visualizing Diffusional Dynamics of Gold Nanorods on Cell Membrane using Single Nanoparticle Darkfield Microscopy

Analyzing the diffusional dynamics of nanoparticles on cell membrane plays a significant role in better understanding the cellular uptake process and provides a theoretical basis for the rational design of nano-medicine delivery. Single particle tracking (SPT) analysis could probe the position and orientation of individual nanoparticles on cell membrane, and reveal their translational and rotational states. Here, we show how to use traditional dark-field microscopy to monitor the dynamics of gold nanorods (AuNRs) on live cell membrane. We also show how to extract the location and orientation of AuNRs using ImageJ and MATLAB, and how to characterize the diffusive states of AuNRs. Statistical analysis of hundreds of particles show that single AuNRs perform Brownian motion on the surface of U87 MG cell membrane. However, individual long trajectory analysis shows that AuNRs have two distinctly different types of motion states on the membrane, namely long-range transport and limited-area confinement. Our SPT methods can be potentially used to study the surface or intracellular particle diffusion in different biological cells and can become a powerful tool for investigations of complex cellular mechanisms.

Here, we show the use of traditional dark-field microscopy to monitor the dynamics of gold nanorods (AuNRs) on cell membrane. The location and orientation of single AuNRs are detected using ImageJ and MATLAB, and the diffusive states of AuNRs are characterized by single particle tracking analysis.

Analyzing the diffusional dynamics of nanoparticles on cell membrane plays a significant role in better understanding the cellular uptake process and ...

Imaging of Podocytic Proteins Nephrin, Actin, and Podocin with Expansion Microscopy

Disruption of the glomerular filter composed of the glomerular endothelium, glomerular basement membrane and podocytes, results in albuminuria. Podocyte foot processes contain actin bundles that bind to cytoskeletal adaptor proteins such as podocin. Those adaptor proteins, such as podocin, link the backbone of the glomerular slit diaphragm, such as nephrin, to the actin cytoskeleton. Studying the localization and function of these and other podocytic proteins is essential for the understanding of the glomerular filter&#39;s role in health and disease. The presented protocol enables the user to visualize actin, podocin, and nephrin in cells with super resolution imaging on a conventional microscope. First, cells are stained with a conventional immunofluorescence technique. All proteins within the sample are then covalently anchored to a swellable hydrogel. Through digestion with proteinase K, structural proteins are cleaved allowing isotropical swelling of the gel in the last step. Dialysis of the sample in water results in a 4-4.5-fold expansion of the sample and the sample can be imaged via a conventional fluorescence microscope, rendering a potential resolution of 70 nm.

The presented method enables visualization of fluorescently labeled cellular proteins with expansion microscopy leading to a resolution of 70 nm on a conventional microscope.

Disruption of the glomerular filter composed of the glomerular endothelium, glomerular basement membrane and podocytes, results in albuminuria. Podocyte ...

Myosin-Specific Adaptations of In vitro Fluorescence Microscopy-Based Motility Assays

Myosin proteins bind and interact with filamentous actin (F-actin) and are found in organisms across the phylogenetic tree. Their structure and enzymatic properties are adapted for the particular function they execute in cells. Myosin 5a processively walks on F-actin to transport melanosomes and vesicles in cells. Conversely, nonmuscle myosin 2b operates as a bipolar filament containing approximately 30 molecules. It moves F-actin of opposite polarity toward the center of the filament, where the myosin molecules work asynchronously to bind actin, impart a power stroke, and dissociate before repeating the cycle. Nonmuscle myosin 2b, along with its other nonmuscle myosin 2 isoforms, has roles that include&#160;cell adhesion, cytokinesis, and tension maintenance. The mechanochemistry of myosins can be studied by performing in vitro motility assays using purified proteins. In the gliding actin filament assay, the myosins are bound to a microscope coverslip surface and translocate fluorescently labeled F-actin, which can be tracked. In the single molecule/ensemble motility assay, however, F-actin is bound to a coverslip and the movement of fluorescently labeled myosin molecules on the F-actin is observed. In this report, the purification of recombinant myosin 5a from Sf9 cells using affinity chromatography is outlined. Following this, we outline two fluorescence microscopy-based assays: the gliding actin filament assay and the inverted motility assay. From these assays, parameters such as actin translocation velocities and single molecule run lengths and velocities can be extracted using the image analysis software. These techniques can also be applied to study the movement of single filaments of the nonmuscle myosin 2 isoforms, discussed herein in the context of nonmuscle myosin 2b. This workflow represents a protocol and a set of quantitative tools that can be used to study the single molecule and ensemble dynamics of nonmuscle myosins.

Presented here is a procedure to express and purify myosin 5a followed by a discussion of its characterization, using both ensemble and single molecule in vitro fluorescence microscopy-based assays, and how these methods can be modified for the characterization of nonmuscle myosin 2b.

Myosin proteins bind and interact with filamentous actin (F-actin) and are found in organisms across the phylogenetic tree. Their structure and enzymatic ...

Simultaneous Visualization of the Dynamics of Crosslinked and Single Microtubules In Vitro by TIRF Microscopy

Microtubules are polymers of &#945;&#946;-tubulin heterodimers that organize into distinct structures in cells. Microtubule-based architectures and networks often contain subsets of microtubule arrays that differ in their dynamic properties. For example, in dividing cells, stable bundles of crosslinked microtubules coexist in close proximity to dynamic non-crosslinked microtubules. TIRF-microscopy-based in vitro reconstitution studies enable the simultaneous visualization of the dynamics of these different microtubule arrays. In this assay, an imaging chamber is assembled with surface-immobilized microtubules, which are either present as single filaments or organized into crosslinked&#160;bundles. Introduction of tubulin, nucleotides, and protein regulators allows direct visualization of associated proteins and of dynamic properties of single and crosslinked microtubules. Furthermore, changes that occur as dynamic single microtubules organize into bundles can be monitored in real-time. The method described here allows for a systematic evaluation of the activity and localization of individual proteins, as well as synergistic effects of protein regulators on two different microtubule subsets under identical experimental conditions, thereby providing mechanistic insights that are inaccessible by other methods.

Simultaneous Visualization of the Dynamics of Crosslinked and Single Microtubules In Vitro by TIRF Microscopy

Here, a TIRF microscopy-based in vitro reconstitution assay is presented to simultaneously quantify and compare the dynamics of two microtubule populations. A method is described to simultaneously view the collective activity of multiple microtubule-associated proteins on crosslinked microtubule bundles and single microtubules.

Microtubules are polymers of &#945;&#946;-tubulin heterodimers that organize into distinct structures in cells. Microtubule-based architectures and ...

Simultaneous Interference Reflection and Total Internal Reflection Fluorescence Microscopy for Imaging Dynamic Microtubules and Associated Proteins

Several techniques have been employed for the direct visualization of cytoskeletal filaments and their associated proteins. Total-internal-reflection-fluorescence (TIRF) microscopy has a high signal-to-background ratio, but it suffers from photobleaching and photodamage of the fluorescent proteins. Label-free techniques such as interference reflection microscopy (IRM) and interferometric scattering microscopy (iSCAT) circumvent the problem of photobleaching but cannot readily visualize single molecules. This paper presents a protocol for combining IRM with a commercial TIRF microscope for the simultaneous imaging of microtubule-associated proteins (MAPs) and dynamic microtubules in vitro. This protocol allows for high-speed observation of MAPs interacting with dynamic microtubules. This improves on existing two-color TIRF setups by eliminating both the need for microtubule labeling and the need for several additional optical components, such as a second excitation laser. Both channels are imaged on the same camera chip to avoid image registration and frame synchronization problems. This setup is demonstrated by visualizing single kinesin molecules walking on dynamic microtubules.

We present a protocol for implementing interference-reflection microscopy and total-internal-reflection-fluorescence microscopy for the simultaneous imaging of dynamic microtubules and fluorescently labeled microtubule-associated proteins.

Several techniques have been employed for the direct visualization of cytoskeletal filaments and their associated proteins. ...

Using Microfluidics and Fluorescence Microscopy to Study the Assembly Dynamics of Single Actin Filaments and Bundles

In order to decipher the complex molecular mechanisms that regulate the assembly and disassembly of actin filaments, it is a great asset to monitor individual reactions live in well-controlled conditions. To do so, live single-filament experiments have emerged over the past 20 years, mostly using total internal reflection fluorescence (TIRF) microscopy, and have provided a trove of key results. In 2011, in order to further expand the possibilities of these experiments and to avoid recurring problematic artifacts, we introduced simple microfluidics in these assays. This study details our basic protocol, where individual actin filaments are anchored by one end to the passivated coverslip surface, align with the flow, and can be successively exposed to different protein solutions. We also present the protocols for specific applications and explain how controlled mechanical forces can be applied, thanks to the viscous drag of the flowing solution. We highlight the technical caveats of these experiments and briefly present possible developments based on this technique. These protocols and explanations, along with today&#39;s availability of easy-to-use microfluidics equipment, should allow non-specialists to implement this assay in their labs.

We present protocols for simple actin filament microfluidic assays, in combination with fluorescence microscopy, that allow one to accurately monitor individual actin filaments in real-time while sequentially exposing them to different protein solutions.

In order to decipher the complex molecular mechanisms that regulate the assembly and disassembly of actin filaments, it is a great asset to monitor ...

Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy

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Using Microfluidics and Fluorescence Microscopy to Study the Assembly Dynamics of Single Actin Filaments and Bundles