Name: fluorescence recovery after merging a droplet to measure the two-dimensional diffusion of a phospholipid monolayer
Uploaded: 2015-10-15T15:00:00
Duration: 7 min 54 s
Description: Watch this Scientific Journal Video about Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer at JoVE.com

This work is supported by the KAIST-funded K-Valley RED&#38;B Project for 2014 and the Basic Science Research Program through the National Research Foundation of Korea (NRF- 2012R1A6A3A040395, NRF-2013R1A1A2057708, NRF- 2012R1A1A1011023).

Caution: Refer to material safety data sheets (MSDS) before use of acetone and chloroform which are carcinogenic.
1. Preparation of Phospholipid Monolayer at a Flat Air-water Interface
<ol>
	<li>Formation of a phospholipid monolayer
	<ol>
		<li>Preparation of a phospholipid solution
		<ol>
			<li>Clean a 4 ml vial with a polytetrafluoroethylene coated cap using acetone, ethanol, and deionized water at least three times, and blow nitrogen gas thoroughly into the vial to get rid of water.</li>
			<li>Dissolve 1 mg of phospholipid (e.g., dioleoylphosphatidylcholine, DOPC) to 1 ml of chloroform in the vial to obtain 1 mg/ml of concentration. Perform this procedure in a fume hood for safety. Use lower or higher concentrations of phospholipid solution if necessary.</li>
			<li>Add dye tagged phospholipids (e.g., Rhodamine dipalmitoylphosphatidylethanolamine, Rhodamine DPPE) with less than 1 mol % of the phospholipid solution, in order to visualize the phospholipid monolayer with a fluorescence microscope. Perform this procedure in a fume hood for safety.</li>
			<li>Wrap the vial with a polytetrafluoroethylene tape to prevent solvent evaporation, and store the sample in a freezer at -20 &#176;C.</li>
		</ol>
		</li>
		<li>Deposition of phospholipids onto the air-water interface
		<ol>
			<li>Clean a Petri dish (55 mm in diameter and 12 mm in height) with ethanol, and deionized water at least three times.</li>
			<li>Fill the Petri dish with 10 ml of deionized water to create an air-water interface.</li>
			<li>Spread few microliters of the phospholipid solution with a micro-syringe onto a clean interface to achieve desired surface pressure and wait for at least 30 min&#160;to evaporate the solvent completely, prior to doing the experiment. 
			Note: A Langmuir trough can be used instead of a Petri dish if precise control of surface pressure is necessary.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Surface pressure measurement
	<ol>
		<li>Measure the surface pressure of the phospholipid monolayer with a Wilhelmy plate tensiometer. Wait for at least 30 min to get the filter paper wetted enough if filter paper is used as a Wilhelmy plate. The detailed protocol is available in Kuhn et al.20.</li>
		<li>Adjust the deposited amount of the phospholipid to control the surface pressure precisely. Add 4 &#181;l of the DOPC solution (1 mg/ml) onto the 30.25 cm2&#8211;area of the interface if ~ 5 mN/m of surface pressure is required. 
		Note: If the filter paper is not fully wetted, surface pressure changes dramatically during the first 30 min of the experiment due to the weight change of the filter paper.</li>
	</ol>
	</li>
	<li>Minimization of the convective flow of the monolayer
	<ol>
		<li>Use a cone-shaped apparatus that contains a 3 mm reservoir with two thin channels, connected to a large section of the Petri dish, to suppress the convective flow of the monolayer, which can disturb morphology imaging and surface pressure measurement.</li>
		<li>Make sure to match the water levels between the inside and outside of the cone-shape apparatus to ensure that phospholipids move freely over the whole region before depositing phospholipids onto the air-water interface.</li>
	</ol>
	</li>
</ol>
2. Preparation of Phospholipid Monolayer at the Curved Surface of a Droplet
<ol>
	<li>Tapering process of a glass capillary using micropipette puller
	<ol>
		<li>Place a glass capillary (o.d. 1 mm, i.d. 0.78 mm, length 100 mm) on a capillary holder of a micropipette puller.</li>
		<li>Design a program for pulling the capillaries with appropriate parameter values (Heat: Ramp, Pull: 60, Vel: 70, Delay: 70 and Pressure 200) and pull the capillaries with the designed program according to manufacturer&#8217;s protocol. 
		Note: A capillary end with a few micrometers-diameter is necessary to form a 100 &#181;m-droplet by applying a pressure with ~ 10 kPa. If the tip end of the capillary is too small, much higher pressure, &#62; 600 kPa, is required to obtain the droplet, while it is hard to control the size of the droplets with a too large capillary tip end.</li>
	</ol>
	</li>
	<li>Absorption of phospholipids onto the droplet surface 
	Note: To form a phospholipid monolayer at the curved interface of a droplet, a phospholipid solution without dye tagged phospholipids is used to obtain an intensity contrast, against the flat monolayer, prepared by procedure 1. In addition, both procedures 2.2.1 and 2.2.2 are allowable here. If precise control of the surface pressure at the droplet surface is necessary, procedure 2.2.2 is highly recommended. However, if not, procedure 2.2.1, which is a much easier way than procedure 2.2.2, is useful.
	<ol>
		<li>Coating process of phospholipids at a tip end
		<ol>
			<li>Clean a slide glass using acetone, ethanol, and deionized water at least three times.</li>
			<li>Place the tapered capillary on a cleaned slide glass, and tilt the capillary to facilitate touching the slide glass with a tip end.</li>
			<li>Drop a few droplets of phospholipid solution (1 mg/ml) onto the tip end of a capillary that is adhered to the glass slide using a glass syringe, and wait at least 30 min to evaporate the solvent completely. 
			Note: It is highly recommended to adhere the tip end of the capillary to the glass slide during procedure 2.2.1.3 because the perimeter of the tip end is too small to hold the droplet of the phospholipids at the tip end only by capillary force.</li>
		</ol>
		</li>
		<li>Preparation of a vesicle solution
		<ol>
			<li>Clean a vial, and remove water from the vial, as introduced in procedure 1.1.1.1.</li>
			<li>Dry a 2 ml volume of phospholipid solution (1 mg/ml) by applying nitrogen gas gently, and desiccate the vial for 1 hr at RT to eliminate any remaining solvent. Perform this procedure in a fume hood for safety.</li>
			<li>Add 2 ml of deionized water into the vial containing dried lipids, and incubate the vial in an oven at 60 &#176;C for 1 hr.</li>
			<li>Shake the vial several times, and sonicate (HF-frequency: Up to 40 kHz, Power: 370 W) for 30 min to obtain vesicles.</li>
			<li>Perform extrusion and freeze-thaw processes to obtain monodisperse unilamellar vesicles. The detailed protocol for preparing vesicles is described in Mayer et al.21. 
			Note: Surface pressure of the droplet interface is controlled precisely by adjusting the waiting time after formation of the droplet that contains monodisperse unilamellar vesicles. Using a pendant drop method22, it is necessary to measure the change of surface pressure according to time, prior to doing the experiment.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Formation of a droplet that contains a phospholipid monolayer at the curved surface
	<ol>
		<li>Fill in the tapered capillary with 10 &#181;l of deionized water from procedure 2.2.1. Alternatively, use 10 &#181;l of the vesicle solution from procedure 2.2.2.</li>
		<li>Connect the capillary to an automated micro-injector to provide the pressure to form the droplet.</li>
		<li>Mount the capillary that is connected to a micro-injector to a micromanipulator to control the position of the capillary precisely.</li>
		<li>Prepare a bright field microscope (Microscope 1, objective lens: 10X NA 0.3) for imaging the lateral view of the capillary with a CCD camera. Microscope 1 thus enables to observe the precise position of the droplet along the z-axis and estimate the size of the droplet.</li>
		<li>Move the tip end to a position where the lateral view of the tip end is well visualized by Microscope 1 using a micromanipulator, and apply a variable pressure (~ 100 hPa) with the tip end of the capillary, until an appropriate size (~100 &#181;m in diameter) of droplet is formed. 
		Note: It is recommended that automated micro-injector and micromanipulator be used, if fine control of the droplet size and location of the droplet is necessary. It is also possible to use manual ones.</li>
	</ol>
	</li>
</ol>
3. Imaging Fluorescence Recovery after Droplet Merging
Note: The fundamental principles of this protocol are identical to those of the FRAP technique, except for the drop coalescence process. The detailed protocol and related theories of FRAP are available in A. Lopez et al.15 and D. Axelrod et al.16.
<ol>
	<li>Monitoring and controlling the location of the droplet
	<ol>
		<li>Prepare an inverted microscope set (Microscope 2, objective lens: 10X NA 0.3, tube lens: focal length 17 cm) that enables both a fluorescence microscope with a proper filter set for Rhodamine-DPPEs (excitation at 560 nm, emission at 583 nm) and a bright field microscope. Use a CCD camera here for visualizing the top views of the droplet with a fluorescence microscope mode and a bright-field microscope mode.</li>
		<li>Move the droplet coated with a phospholipid to a flat air-water interface along the z-axis, but do not merge the droplet yet, using the micromanipulator. Use Microscope 1 to visualize the lateral view of the droplet.</li>
		<li>Locate the droplet at the center of the top view of the flat monolayer, using the micromanipulator. Use the bright-field microscope mode of Microscope 2 to visualize top view of flat monolayer.</li>
	</ol>
	</li>
	<li>Merging the droplet onto the flat air-water interface
	<ol>
		<li>Move the droplet further toward the flat interface until the droplet merges onto the interface, using the micromanipulator. If the merging process is done successfully, a dark region with a circular shape that is surrounded by a white background, is observed using the fluorescence mode of Microscope 2.</li>
		<li>Record the series of fluorescent images according to time after merging the droplet, using the fluorescence mode of Microscope 2. Use a faster frame rate than the diffusion time scale of the monolayer here. In DOPC monolayer, it takes a few minutes to diffuse into the 200 &#181;m-dark area completely.</li>
	</ol>
	</li>
</ol>
4. Determining the Diffusion Coefficient by Image Analysis
Note: To determine the diffusion coefficient from a series of images, customized program for image analysis is built as described below. A detailed source code of this program is available in JoVE website.
<ol>
	<li>Detection of a circular region of interest
	<ol>
		<li>Detection of the center of the region of interest
		<ol>
			<li>Obtain a series of fluorescent images that have been recorded during a recovery process which contains a circular dark area and a white background, and set the first image of the series as a reference image. Here, RD is the radius of the dark area in a reference image.</li>
			<li>Convolute the reference image with a white circle whose intensity is uniform over a whole region. Use embedded function named &#8216;conv2&#8217; for convolution as shown in the source code of the customized program line 124. Here, the radius of the white circle is slightly smaller than RD.</li>
			<li>Find a position that indicates a minimum value in the convolution calculation, and set this position as the center of the region of interest in the reference image.</li>
		</ol>
		</li>
		<li>Determining a radius of the region of interest
		<ol>
			<li>Convolute the reference image with a white circle that contains a center position, determined by a procedure 4.1 and uniform intensity over a whole region. Here, RS is the radius of the white circle. Use iteration such as &#8216;for&#8217; or &#8216;while&#8217; with equation of a circle to make the white circle as shown in the source code of the customized program line 102 to 109.</li>
			<li>Convolute the reference image with another white circle which has a slightly larger radius (5%&#8211;10%), RL, than RS. Use same method with procedure 4.1.2.1 to make the circle as shown in the source code of the customized program line 113 to 120.</li>
			<li>Obtain the difference in value between the two convolution calculations of 4.1.2.1 and 4.1.2.2.</li>
			<li>Repeat the above procedures from RS = RD/2 to RS = 2RD, by increasing both the RS and RL with a pixel level. Make an iteration that contains whole source codes from procedure 4.1.2.1 to 4.1.2.3 to repeat.</li>
			<li>Find the radius of RS that indicates the maximum difference in value between the two convolution calculations. Use embedded function named &#8216;max&#8217; to find the radius indicates the maximum difference in value as shown in the source code of the customized program line 148 to 149. This RS thus indicates the radius of the dark area in the reference image.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Calculation of a fractional intensity
	<ol>
		<li>Set a circle that contains a center position and a radius, determined by procedure 4.1 as a region of interest.</li>
		<li>Calculate the average intensities of the region of interest in a series of fluorescence images according to time. Convolute each frame with region of interest and divide it by area of region of interest to calculate the average intensity. The details are available in the source code of the customized program which is available in JoVE website.</li>
		<li>Calculate a fractional intensity, defined as the equation below, where F(t) is the average intensity in the circle that is a region of interest according to time, Fi is the initial intensity in the circle, and Fo is the intensity of a white background. 
		f(t) = (F(t) &#8211; Fi)/(Fo &#8211; Fi)&#160;&#160;&#160;&#160;&#160; (Equation 1).</li>
	</ol>
	</li>
	<li>Fitting the fractional intensity to FRAP theory
	<ol>
		<li>Fit the fractional intensity with the equation below, where &#964; is a characteristic diffusion time and I0, I1 are modified Bessel functions, using a fitting program, and obtain &#964; 
		<img alt="Equation 2" src="/files/ftp_upload/53376/53376eq2.jpg" />&#160;&#160;&#160;&#160;&#160; (Equation 2).</li>
		<li>Obtain a diffusion coefficient based on the relation, &#964; = a2/4D, where D is the diffusion coefficient and a is the radius of the dark area. 
		Note: During the fitting process, it is possible to shift the fractional intensity profile along a time axis when the recovery process has already started, before recording the images.</li>
	</ol>
	</li>
</ol>

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The authors declare no competing financial interest.

FRAM shares a lot of fundamental principles with FRAP, especially for measuring fluorescence recovery after bleaching a specific area, but FRAM uses a process of merging a droplet onto the flat interface to form a bleached area, instead of applying an intensive light. The merging process is thus most important step in FRAM, and especially, the shape of the dark stain at the flat monolayer after merging a droplet determines the accuracy of the diffusivity measurement. Specifically, based on a current method, we only set the circle with a radius R as a region of interest to calculate the average intensity of the dark stain, shown in procedure 4, and if there is a too much deviation from the circular shape, this would disturb the precise measurement of a diffusion coefficient. Therefore, it is necessary to obtain a circular shaped dark region, but, noncircular shapes are formed occasionally due to several reasons. First, if there exists a convective flow in the Petri dish, the shape of the dark area becomes elongated along the direction of flow. As mentioned in procedure 1.3, a cone-shape apparatus helps to suppress the convective flow, and this elongation would be minimized. Second, if the tip end of the capillary touches the flat interface during a merging process, the dark area is formed with a variety of shapes since the capillary end interrupts the merging process. By obtaining a droplet that is only hanging from the very end of the capillary, this interruption can be prevented. In particular, a hydrophobic treatment of the capillary helps the droplet to sit at the very end of the capillary. Therefore, above trouble shootings and modifications enable us to measure diffusion properties more precisely.
This well troubleshot process thus allows FRAM to have several significant advantages over FRAP. First, FRAM requires simpler equipment compared to FRAP. For FRAM, it is sufficient to use a simple fluorescence microscope, instead of an expensive confocal microscope with a high power laser whose wavelength must match with the absorption spectrum of the dye. In addition, it is necessary to use additional apparatus to adjust the size to the bleached area in the FRAP, while the FRAM controls the size of the area easily by adjusting the size of the droplet, or the surface pressure at the droplet surface. Second, it is possible to use various species of dyes in FRAM. FRAP only uses dye molecules whose bleaching process is much faster than the diffusion process. If the diffusion of the dyes occurs during the bleaching process, it is hard to estimate the diffusion property accurately. The FRAM, however, does not require a process for bleaching dyes and this thus enables the use of various types of dyes in the fluorescence imaging. In addition, the FRAP requires additional high power lasers and filter sets to change the dye species, while it is only necessary to replace the filter sets in the FRAM. Finally, since the monolayers at the droplet surface and the flat interface can be formed independently, thus enabling the study of inter-diffusion or mixing between two different lipid monolayers by merging A-type monolayer to B-type monolayer, while the FRAP only measures the self-diffusion of a monolayer.
Despite these advantages, the process of merging a droplet onto a flat air-water interface can potentially limit this technique due to several issues that might be of concern, such as a surface pressure mismatch between the two monolayers, the time scale of the merging process, and an increase in the surface pressure of the flat monolayer after merging droplets. These issues, however, do not affect the diffusion measurement significantly for the following reasons. First, even though the surface pressures at the two different monolayers are quite different, an equilibration process is completed at a very early stage during the recovery process. For example, if the surface pressure of the monolayer at the droplet surface is higher than that of the monolayer at the flat air-water interface, the dark area expands until the surface pressure equilibrates. Since this process is completed within 10 msec, the surface pressure will be equilibrated before it affects the diffusion process significantly. Second, if the time scale of the merging process is fast enough, it does not limit the diffusion measurement at all. Fortunately, a typical merging process is also completed within 10 msec. Finally, even multiple merging of the droplets onto the flat interface do not increase the surface pressure since the surface area of the trough is far larger than the surface area of the droplet. According to the sizes of the trough and the droplets, described in the protocol, the area per molecule increases less than 0.015% by merging a droplet. Accordingly, the increase of surface pressure due to the change of area per molecule is less than 0.1%, which is negligible because it is much smaller than the typical error in surface pressure, as measured by Wilhelmy plate tensiometer.
In summary, we introduced a new method to measure the lateral diffusion property of a phospholipid monolayer by merging a droplet monolayer onto the flat interface. This technique requires relatively simple equipment and also enables the use of various sorts of dye species. The FRAM is thus potentially applicable for diffusion measurement of any surface active agents, including phospholipids, block copolymers, proteins and even nanoparticles at a fluid-fluid interface. Furthermore, we expect that the FRAM provides a new way to study the inter-diffusion or mixing between two different surface active agents.

Phospholipids are major components of cell membranes and the membranes of organelles, and the fluidity of these membrane layers often affects cellular functions by altering the activity of membrane proteins1&#8211;3. For instance, membrane&#160;lipid&#160;homeostasis&#160;is achieved by regulating membrane fluidity, which is detected by membrane proteins, and an abnormal level of fluidity causes severe diseases, such as hepatic steatosis and cholestasis4. In addition, fluidity of a phospholipid monolayer at the air-alveoli fluid interface has important implications in its functions. High fluidity of the lung surfactant phospholipid monolayer facilitates spreading of the layer during inhalation, whereas a low fluidity enables the layer to stay within the alveoli during exhalation5,6. It is thus important to estimate the fluidity of the phospholipid layers to understand their roles.
A direct measure of the fluidity is viscosity, and the viscosity of phospholipid layers has been measured by using micron-sized colloids7, magnetic needles8,9, and magnetic micro-buttons6,10,11. However, these techniques are limited to relatively rigid films, and cannot measure less viscous films. For such cases, diffusivity would be an alternative to quantify fluidity of phospholipid layers. For several decades, a variety of techniques to measure the diffusion properties of phospholipid layers have been developed, such as fluorescence quenching method12, pulsed field gradient NMR13, and fluorescence correlation spectroscopy (FCS)14. One of the most representative methods is fluorescence recovery after photobleaching (FRAP)15,16. Due to the simplicity of the measurement procedure and related theories, several studies on the diffusion properties of phospholipid layers have been performed using FRAP17&#8211;19. However, FRAP usually requires an expensive confocal microscope setup with a high-power laser.
Here, we present a new technique to measure the lateral diffusion of phospholipid monolayers, termed as fluorescence recovery after merging (FRAM). The key difference between FRAP and FRAM is that the photobleaching step is replaced by the drop coalescence. Merging a droplet covered by non-fluorescence monolayer onto a fluorescently labeled flat monolayer leaves a circular dark stain on a bright flat monolayer, thus setting up the same initial state with the photobleaching step. We then observe the fluorescence recovery in the dark stain with time to measure the lateral diffusivity. This new &#8220;bleaching&#8221; step by drop coalescence provides significant advantages over FRAP: FRAM only requires a fluorescence microscope rather than an expensive confocal microscope with a high power laser that is necessary for FRAP. In addition, FRAM has a wide selection of fluorescence dyes since it does not involve the photobleaching process. Finally, the two different monolayers, a droplet monolayer and a flat monolayer, can be prepared independently, thus allowing interdiffusion to be measured, while FRAP only measures the self-diffusion of monolayers.
FRAM provides a wide range of diffusion measurements from highly viscous materials to nearly inviscid materials. In principal, FRAM can measure the maximum diffusivity of 106 &#181;m2/sec, which is comparable to existing techniques, when the diffusion occurs across the area 100 &#181;m by 100 &#181;m during the time for the drop coalescence process (~ 10 msec). Furthermore, slow diffusion process can be easily measured unless monolayers are solid. FRAM can be used for any kinds of surface active materials as long as appropriate fluorescently tagged molecules are available.

<table border="0" cellpadding="0" cellspacing="0" width="1288">
	<colgroup>
		<col />
		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="22">
			<td height="22" style="height:22px;width:216px;">Acetone</td>
			<td style="width:269px;">OCI corporation</td>
			<td style="width:251px;">Acetone 3.8L Extra Pure</td>
			<td style="width:552px;">Purity: &#8805; 99.5%, Please consult material safety data sheets (MSDS) before use.</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Ethanol</td>
			<td>OCI corporation</td>
			<td>Ethanol 3.8L Extra Pure</td>
			<td>Purity: &#8805; 94%, Please consult material safety data sheets (MSDS) before use.</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Deionized water/Water purify system</td>
			<td>Millipore</td>
			<td>Milli-Q liocel</td>
			<td>&#62;18.2 M&#937;&#903;cm</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dioleoylphosphatidylcholine, DOPC</td>
			<td>Avanti Polar Lipids</td>
			<td>850375C</td>
			<td>Please consult material safety data sheets (MSDS) before use. Chloroform is carcinogenic.</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Chloroform</td>
			<td>LiChrosolv</td>
			<td>Chloroform ultrapure (A3633)</td>
			<td>Purity: &#8805; 99.8%, Please consult material safety data sheets (MSDS) before use. Carcinogenic</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Rhodamine DPPE</td>
			<td>Avanti Polar Lipids</td>
			<td>810158C, 810158P</td>
			<td>Avoid direct light exposure to prevent photobleaching</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Wilhelmy plate tensiometer</td>
			<td>R&#38;K ultrathin organic film technology</td>
			<td>Wilhelmy tensiometer</td>
			<td>http://www.rieglerkirstein.de/index.htm</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Micropipette puller</td>
			<td>Sutter instrument</td>
			<td>P-1000</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Micro-injector</td>
			<td>Eppendorf</td>
			<td>Femtojet</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Micromanipulator</td>
			<td>Eppendorf</td>
			<td>Micromanipulator 5171</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Microscope 1</td>
			<td>Objective lens: Olympus</td>
			<td>Objective lens: UPlanFl 10x</td>
			<td>Objective lens: 10x NA 0.3</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Microscope 2</td>
			<td>Objective lens: Olympus, Tube lens: Thorlabs</td>
			<td>Objective lens: UPlanFl 10x</td>
			<td>Objective lens: 10x NA 0.3, tube lens: focal length 17 cm</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">CCD for Microscope 1</td>
			<td>Jai</td>
			<td>CV 950 camera</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">CCD for Microscope 2</td>
			<td>Andor</td>
			<td>iXon3 EMCCD</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Filter set</td>
			<td>Chroma technology</td>
			<td>Catalog Set 49004: ET545, T565, ET605</td>
			<td>Prepare suitable for dye molecules</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Sonicator</td>
			<td>DAIHAN Scientific</td>
			<td>Wiseclean WUC-D06H</td>
			<td></td>
		</tr>
	</tbody>
</table>

fluorescence recovery after merging a droplet to measure the two-dimensional diffusion of a phospholipid monolayer

We introduce a new method to measure the lateral diffusivity of a surfactant monolayer at the fluid-fluid interface, called fluorescence recovery after merging (FRAM). FRAM adopts the same principles as the fluorescence recovery after photobleaching (FRAP) technique, especially for measuring fluorescence recovery after bleaching a specific area, but FRAM uses a drop coalescence instead of photobleaching dye molecules to induce a chemical potential gradient of dye molecules. Our technique has several advantages over FRAP: it only requires a fluorescence microscope rather than a confocal microscope equipped with high power lasers; it is essentially free from the selection of fluorescence dyes; and it has far more freedom to define the measured diffusion area. Furthermore, FRAM potentially provides a route for studying the mixing or inter-diffusion of two different surfactants, when the monolayers at a surface of droplet and at a flat air/water interface are prepared with different species, independently.

A series of fluorescence images were obtained with time during the recovery process after merging a droplet coated with a DOPC monolayer onto a flat DOPC monolayer, as listed in Figure 1. The DOPC monolayer at the flat air-water interface was doped with low amounts of Rhodamine-DPPE, and this thus made it possible to visualize a background with a bright color and a dark region newly added to the flat interface. There, a recovery process was observed at 23 mN/m of fixed surface pressure. A fit of equation 1 to the change of fractional intensity according to time is shown in Figure 2. The R2 value of this fit is 0.999, and this fit still works well even at lower or higher surface pressures. The diffusion coefficient of the DOPC monolayer obtained from this fit was 27.54 &#181;m2/sec at 23 mN/m of surface pressure.
For further validation of the FRAM, diffusion coefficients of the DOPC and dipalmitoylphosphatidylcholine (DPPC) monolayers were measured according to surface pressure. As shown in Figure 3, FRAM captures the rapid decrease of diffusion coefficient of the DPPC monolayer at ~ 9 mN/m of surface pressure, where a LC (liquid condensed) &#8211; LE (liquid expanded) phase transition occurs10, and the values of diffusion coefficients are also agreed well with the previously measurements by Peters et al.19. In addition, an exponential decay of the diffusion coefficient with the surface pressure was observed in the DOPC monolayer, and this tendency is almost identical with the one measured by Caruso et al.12.
<img alt="Figure 1" src="/files/ftp_upload/53376/53376fig1.jpg" /> 
Figure 1. (A) Schematic illustration of the FRAM (fluorescence recovery after merging) technique. As the lipid monolayer coated droplet is merged to flat air-water interface, the lipid monolayer without fluorescence tagged lipid is inserted into flat fluorescent lipid monolayer. (B) Fluorescence microscope images with time during the recovery process of a DOPC monolayer at 23 mN/m of surface pressure (scale bar = 100 &#181;m). The dark region of the DOPC monolayer is fully recovered by the diffusion process within several minutes. <a href="https://www.jove.com/files/ftp_upload/53376/53376fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" src="/files/ftp_upload/53376/53376fig2.jpg" /> 
Figure 2. Fractional intensity vs. time. Black circles and the gray dotted line indicate the values of fractional intensities obtained from image analysis (procedures 4.1 and 4.2) and the fit of equation 1 to the fractional intensities with time, shown in procedure 4.3, respectively. <a href="https://www.jove.com/files/ftp_upload/53376/53376fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/53376/53376fig3.jpg" /> 
Figure 3. Diffusion coefficients of DOPC (triangle) and DPPC (empty square) monolayers as a function of surface pressure. The lines with the bright gray color and with the dark gray color indicate the values of the diffusion coefficient previously reported by Peters et al. and Caruso et al., respectively. This figure has been modified from Jeong et al.23. Reprinted with permission from Jeong et al. Langmuir. 30(48), 14369-14374. Copyright 2014 American Chemical Society. <a href="https://www.jove.com/files/ftp_upload/53376/53376fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer at JoVE.com

Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer

We present a new technique to measure the lateral diffusion of a surface active species at the fluid-fluid interface by merging a droplet monolayer onto a flat monolayer.

We introduce a new method to measure the lateral diffusivity of a surfactant monolayer at the fluid-fluid interface, called fluorescence recovery after ...

fluorescence-recovery-after-merging-droplet-to-measure-two

Research

JoVE Journal

Bioengineering

Creating Two-Dimensional Patterned Substrates for Protein and Cell Confinement

Microcontact printing provides a rapid, highly reproducible method for the creation of well-defined patterned substrates.1 While microcontact printing can be employed to directly print a large number of molecules, including proteins,2 DNA,3 and silanes,4 the formation of self-assembled monolayers (SAMs) from long chain alkane thiols on gold provides a simple way to confine proteins and cells to specific patterns containing adhesive and resistant regions. This confinement can be used to control cell morphology and is useful for examining a variety of questions in protein and cell biology. Here, we describe a general method for the creation of well-defined protein patterns for cellular studies.5 This process involves three steps: the production of a patterned master using photolithography, the creation of a PDMS stamp, and microcontact printing of a gold-coated substrate. Once patterned, these cell culture substrates are capable of confining proteins and/or cells (primary cells or cell lines) to the pattern.
The use of self-assembled monolayer chemistry allows for precise control over the patterned protein/cell adhesive regions and non-adhesive regions; this cannot be achieved using direct protein stamping. Hexadecanethiol, the long chain alkane thiol used in the microcontact printing step, produces a hydrophobic surface that readily adsorbs protein from solution. The glycol-terminated thiol, used for backfilling the non-printed regions of the substrate, creates a monolayer that is resistant to protein adsorption and therefore cell growth.6 These thiol monomers produce highly structured monolayers that precisely define regions of the substrate that can support protein adsorption and cell growth. As a result, these substrates are useful for a wide variety of applications from the study of intercellular behavior7 to the creation of microelectronics.8
While other types of monolayer chemistry have been used for cell culture studies, including work from our group using trichlorosilanes to create patterns directly on glass substrates,9 patterned monolayers formed from alkane thiols on gold are straight-forward to prepare. Moreover, the monomers used for monolayer preparation are commercially available, stable, and do not require storage or handling under inert atmosphere. Patterned substrates prepared from alkane thiols can also be recycled and reused several times, maintaining cell confinement.10

Self-assembled monolayers (SAMs) formed from long chain alkane thiols on gold provide well-defined substrates for the formation of protein patterns and cell confinement. Microcontact printing of hexadecanethiol using a polydimethylsiloxane (PDMS) stamp followed by backfilling with a glycol-terminated alkane thiol monomer produces a pattern where protein and cells adsorb only to the stamped hexadecanethiol region.

Microcontact printing provides a rapid, highly reproducible method for the creation of well-defined patterned substrates.1  While microcontact printing ...

Design of a Cyclic Pressure Bioreactor for the Ex Vivo Study of Aortic Heart Valves

The aortic valve, located between the left ventricle and the aorta, allows for unidirectional blood flow, preventing backflow into the ventricle. Aortic valve leaflets are composed of interstitial cells suspended within an extracellular matrix (ECM) and are lined with an endothelial cell monolayer. The valve withstands a harsh, dynamic environment and is constantly exposed to shear, flexion, tension, and compression. Research has shown calcific lesions in diseased valves occur in areas of high mechanical stress as a result of endothelial disruption or interstitial matrix damage1-3. Hence, it is not surprising that epidemiological studies have shown high blood pressure to be a leading risk factor in the onset of aortic valve disease4. 
The only treatment option currently available for valve disease is surgical replacement of the diseased valve with a bioprosthetic or mechanical valve5. Improved understanding of valve biology in response to physical stresses would help elucidate the mechanisms of valve pathogenesis. In turn, this could help in the development of non-invasive therapies such as pharmaceutical intervention or prevention. Several bioreactors have been previously developed to study the mechanobiology of native or engineered heart valves6-9. Pulsatile bioreactors have also been developed to study a range of tissues including cartilage10, bone11 and bladder12. The aim of this work was to develop a cyclic pressure system that could be used to elucidate the biological response of aortic valve leaflets to increased pressure loads. 
The system consisted of an acrylic chamber in which to place samples and produce cyclic pressure, viton diaphragm solenoid valves to control the timing of the pressure cycle, and a computer to control electrical devices. The pressure was monitored using a pressure transducer, and the signal was conditioned using a load cell conditioner. A LabVIEW program regulated the pressure using an analog device to pump compressed air into the system at the appropriate rate. The system mimicked the dynamic transvalvular pressure levels associated with the aortic valve; a saw tooth wave produced a gradual increase in pressure, typical of the transvalvular pressure gradient that is present across the valve during diastole, followed by a sharp pressure drop depicting valve opening in systole. The LabVIEW program allowed users to control the magnitude and frequency of cyclic pressure. The system was able to subject tissue samples to physiological and pathological pressure conditions. This device can be used to increase our understanding of how heart valves respond to changes in the local mechanical environment.

Design of a Cyclic Pressure Bioreactor for the Ex Vivo Study of Aortic Heart Valves

A cyclic pressure bioreactor capable of subjecting heart valve tissue to physiological and pathological pressure conditions has been designed. A LabVIEW program allows users to control pressure magnitude, amplitude and frequency. This device can be used to study the mechanobiology of heart valve tissue or isolated cells.

The aortic valve, located between the left ventricle and the aorta, allows for unidirectional blood flow, preventing backflow into the ventricle. Aortic ...

Fluorescence detection methods for microfluidic droplet platforms

The development of microfluidic platforms for performing chemistry and biology has in large part been driven by a range of potential benefits that accompany system miniaturisation. Advantages include the ability to efficiently process nano- to femoto- liter volumes of sample, facile integration of functional components, an intrinsic predisposition towards large-scale multiplexing, enhanced analytical throughput, improved control and reduced instrumental footprints.1
In recent years much interest has focussed on the development of droplet-based (or segmented flow) microfluidic systems and their potential as platforms in high-throughput experimentation.2-4 Here water-in-oil emulsions are made to spontaneously form in microfluidic channels as a result of capillary instabilities between the two immiscible phases. Importantly, microdroplets of precisely defined volumes and compositions can be generated at frequencies of several kHz. Furthermore, by encapsulating reagents of interest within isolated compartments separated by a continuous immiscible phase, both sample cross-talk and dispersion (diffusion- and Taylor-based) can be eliminated, which leads to minimal cross-contamination and the ability to time analytical processes with great accuracy. Additionally, since there is no contact between the contents of the droplets and the channel walls (which are wetted by the continuous phase) absorption and loss of reagents on the channel walls is prevented.
Once droplets of this kind have been generated and processed, it is necessary to extract the required analytical information. In this respect the detection method of choice should be rapid, provide high-sensitivity and low limits of detection, be applicable to a range of molecular species, be non-destructive and be able to be integrated with microfluidic devices in a facile manner. To address this need we have developed a suite of experimental tools and protocols that enable the extraction of large amounts of photophysical information from small-volume environments, and are applicable to the analysis of a wide range of physical, chemical and biological parameters. Herein two examples of these methods are presented and applied to the detection of single cells and the mapping of mixing processes inside picoliter-volume droplets. We report the entire experimental process including microfluidic chip fabrication, the optical setup and the process of droplet generation and detection.

Droplet-based microfluidic platforms are promising candidates for high throughput experimentation since they are able to generate picoliter, self-compartmentalized vessels inexpensively at kHz rates. Through integration with fast, sensitive and high resolution fluorescence spectroscopic methods, the large amounts of information generated within these systems can be efficiently extracted, harnessed and utilized.

The development of microfluidic platforms for performing chemistry and biology has in large part been driven by a range of potential benefits that ...

Synthesis, Assembly, and Characterization of Monolayer Protected Gold Nanoparticle Films for Protein Monolayer Electrochemistry

Colloidal gold nanoparticles protected with alkanethiolate ligands called monolayer protected gold clusters (MPCs) are synthesized and subsequently incorporated into film assemblies that serve as adsorption platforms for protein monolayer electrochemistry (PME). PME is utilized as the model system for studying electrochemical properties of redox proteins by confining them to an adsorption platform at a modified electrode, which also serves as a redox partner for electron transfer (ET) reactions. Studies have shown that gold nanoparticle film assemblies of this nature provide for a more homogeneous protein adsorption environment and promote ET without distance dependence compared to the more traditional systems modified with alkanethiol self-assembled monolayers (SAM).1-3 In this paper, MPCs functionalized with hexanethiolate ligands are synthesized using a modified Brust reaction4 and characterized with ultraviolet visible (UV-Vis) spectroscopy, transmission electron microscopy (TEM), and proton (1H) nuclear magnetic resonance (NMR). MPC films are assembled on SAM modified gold electrode interfaces by using a "dip cycle" method of alternating MPC layers and dithiol linking molecules. Film growth at gold electrode is tracked electrochemically by measuring changes to the double layer charging current of the system. Analogous films assembled on silane modified glass slides allow for optical monitoring of film growth and cross-sectional TEM analysis provides an estimated film thickness. During film assembly, manipulation of the MPC ligand protection as well as the interparticle linkage mechanism allow for networked films, that are readily adaptable, to interface with redox protein having different adsorption mechanism. For example, Pseudomonas aeruginosa azurin (AZ) can be adsorbed hydrophobically to dithiol-linked films of hexanethiolate MPCs and cytochrome c (cyt c) can be immobilized electrostatically at a carboxylic acid modified MPC interfacial layer. In this report, we focus on the film protocol for the AZ system exclusively. Investigations involving the adsorption of proteins on MPC modified synthetic platforms could further the understanding of interactions between biomolecules and man-made materials, and consequently aid the development of biosensor schemes, ET modeling systems, and synthetic biocompatible materials.5-8

Alkanethiolate stabilized gold colloids known as monolayer protected clusters (MPCs) are synthesized, characterized, and assembled into thin films as an adsorption interface for protein monolayer electrochemistry of simple redox protein like Pseudomonas aeruginosa azurin (AZ) and cytochrome c (cyt c).

Colloidal gold nanoparticles protected with alkanethiolate ligands called monolayer protected gold clusters (MPCs) are synthesized and subsequently ...

3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles

The objective of this video protocol is to discuss how to perform and analyze a three-dimensional fluorescent orbital particle tracking experiment using a modified two-photon microscope1. As opposed to conventional approaches (raster scan or wide field based on a stack of frames), the 3D orbital tracking allows to localize and follow with a high spatial (10 nm accuracy) and temporal resolution (50 Hz frequency response) the 3D displacement of a moving fluorescent particle on length-scales of hundreds of microns2. The method is based on a feedback algorithm that controls the hardware of a two-photon laser scanning microscope in order to perform a circular orbit around the object to be tracked: the feedback mechanism will maintain the fluorescent object in the center by controlling the displacement of the scanning beam3-5. To demonstrate the advantages of this technique, we followed a fast moving organelle, the lysosome, within a living cell6,7. Cells were plated according to standard protocols, and stained using a commercially lysosome dye. We discuss briefly the hardware configuration and in more detail the control software, to perform a 3D orbital tracking experiment inside living cells. We discuss in detail the parameters required in order to control the scanning microscope and enable the motion of the beam in a closed orbit around the particle. We conclude by demonstrating how this method can be effectively used to track the fast motion of a labeled lysosome along microtubules in 3D within a live cell. Lysosomes can move with speeds in the range of 0.4-0.5 &#181;m/sec, typically displaying a directed motion along the microtubule network8.

In this video protocol we track - at high speed and in three dimensions - fluorescently labeled lysosomes within living cells, using the orbital tracking method in a modified two-photon microscope.

The objective of this video protocol is to discuss how to perform and analyze a three-dimensional fluorescent orbital particle tracking experiment using a ...

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope

It has become increasingly evident that the spatial distribution and the motion of membrane components like lipids and proteins are key factors in the regulation of many cellular functions. However, due to the fast dynamics and the tiny structures involved, a very high spatio-temporal resolution is required to catch the real behavior of molecules. Here we present the experimental protocol for studying the dynamics of fluorescently-labeled plasma-membrane proteins and lipids in live cells with high spatiotemporal resolution. Notably, this approach doesn&#8217;t need to track each molecule, but it calculates population behavior using all molecules in a given region of the membrane. The starting point is a fast imaging of a given region on the membrane. Afterwards, a complete spatio-temporal autocorrelation function is calculated correlating acquired images at increasing time delays, for example each 2, 3, n repetitions. It is possible to demonstrate that the width of the peak of the spatial autocorrelation function increases at increasing time delay as a function of particle movement due to diffusion. Therefore, fitting of the series of autocorrelation functions enables to extract the actual protein mean square displacement from imaging (iMSD), here presented in the form of apparent diffusivity vs average displacement. This yields a quantitative view of the average dynamics of single molecules with nanometer accuracy. By using a GFP-tagged variant of the Transferrin Receptor (TfR) and an ATTO488 labeled 1-palmitoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine (PPE) it is possible to observe the spatiotemporal regulation of protein and lipid diffusion on &#181;m-sized membrane regions in the micro-to-milli-second time range.

Spatial distribution and temporal dynamics of plasma membrane proteins and lipids is a hot topic in biology. Here this issue is addressed by a spatio-temporal image fluctuation analysis that provides conceptually the same physical quantities of single particle tracking, but it uses small molecular labels and standard microscopy setups.

It has become increasingly evident that the spatial distribution and the motion of membrane components like lipids and proteins are key factors in the ...

An In Vitro Enzymatic Assay to Measure Transcription Inhibition by Gallium(III) and H3 5,10,15-tris(pentafluorophenyl)corroles

Chemotherapy often involves broad-spectrum cytotoxic agents with many side effects and limited targeting. Corroles are a class of tetrapyrrolic macrocycles that exhibit differential cytostatic and cytotoxic properties in specific cell lines, depending on the identities of the chelated metal and functional groups. The unique behavior of functionalized corroles towards specific cell lines introduces the possibility of targeted chemotherapy.
Many anticancer drugs are evaluated by their ability to inhibit RNA transcription. Here we present a step-by-step protocol for RNA transcription in the presence of known and potential inhibitors. The evaluation of the RNA products of the transcription reaction by gel electrophoresis and UV-Vis spectroscopy provides information on inhibitive properties of potential anticancer drug candidates and, with modifications to the assay, more about their mechanism of action.
Little is known about the molecular mechanism of action of corrole cytotoxicity. In this experiment, we consider two corrole compounds: gallium(III) 5,10,15-(tris)pentafluorophenylcorrole (Ga(tpfc)) and freebase analogue 5,10,15-(tris)pentafluorophenylcorrole (tpfc). An RNA transcription assay was used to examine the inhibitive properties of the corroles. Five transcription reactions were prepared: DNA treated with Actinomycin D, triptolide, Ga(tpfc), tpfc at a [complex]:[template DNA base] ratio of 0.01, respectively, and an untreated control.
The transcription reactions were analyzed after 4 hr using agarose gel electrophoresis and UV-Vis spectroscopy. There is clear inhibition by Ga(tpfc), Actinomycin D, and triptolide.
This RNA transcription assay can be modified to provide more mechanistic detail by varying the concentrations of the anticancer complex, DNA, or polymerase enzyme, or by incubating the DNA or polymerase with the complexes prior to RNA transcription; these modifications would differentiate between an inhibition mechanism involving the DNA or the enzyme. Adding the complex after RNA transcription can be used to test whether the complexes degrade or hydrolyze the RNA. This assay can also be used to study additional anticancer candidates.

An In Vitro Enzymatic Assay to Measure Transcription Inhibition by GalliumIII and H3 5,10,15-trispentafluorophenylcorroles

Gallium(III) 5,10,15-(tris)pentafluorophenylcorrole and its freebase analogue exhibit low micromolar cell cytotoxicity. This manuscript describes an RNA transcription reaction, imaging RNA with an ethidium bromide-stained gel, and quantifying RNA with UV-Vis spectroscopy, in order to assess transcription inhibition by corroles and demonstrates a straightforward method of evaluating anticancer candidate properties.

Chemotherapy often involves broad-spectrum cytotoxic agents with many side effects and limited targeting. Corroles are a class of tetrapyrrolic ...

Planar Gradient Diffusion System to Investigate Chemotaxis in a 3D Collagen Matrix

The importance of cell migration can be seen through the development of human life. When cells migrate, they generate forces and transfer these forces to their surrounding area, leading to cell movement and migration. In order to understand the mechanisms that can alter and/or affect cell migration, one can study these forces. In theory, understanding the fundamental mechanisms and forces underlying cell migration holds the promise of effective approaches for treating diseases and promoting cellular transplantation. Unfortunately, modern chemotaxis chambers that have been developed are usually restricted to two dimensions (2D) and have complex diffusion gradients that make the experiment difficult to interpret. To this end, we have developed, and describe in this paper, a direct-viewing chamber for chemotaxis studies, which allows one to overcome modern chemotaxis chamber obstacles able to measure cell forces and specific concentration within the chamber in a 3D environment to study cell 3D migration. More compelling, this approach allows one to successfully model diffusion through 3D collagen matrices and calculate the coefficient of diffusion of a chemoattractant through multiple different concentrations of collagen, while keeping the system simple and user friendly for traction force microscopy (TFM) and digital volume correlation (DVC) analysis.

Cell migration is an important part of human development and life. In order to understand the mechanisms that can alter cell migration, we present a planar gradient diffusion system to investigate chemotaxis in a 3D collagen matrix, which allows one to overcome modern diffusion chamber limitations of existing assays.

The importance of cell migration can be seen through the development of human life. When cells migrate, they generate forces and transfer these forces to ...

Multicolor Fluorescence Detection for Droplet Microfluidics Using Optical Fibers

Fluorescence assays are the most common readouts used in droplet microfluidics due to their bright signals and fast time response. Applications such as multiplex assays, enzyme evolution, and molecular biology enhanced cell sorting require the detection of two or more colors of fluorescence. Standard multicolor detection systems that couple free space lasers to epifluorescence microscopes are bulky, expensive, and difficult to maintain. In this paper, we describe a scheme to perform multicolor detection by exciting discrete regions of a microfluidic channel with lasers coupled to optical fibers. Emitted light is collected by an optical fiber coupled to a single photodetector. Because the excitation occurs at different spatial locations, the identity of emitted light can be encoded as a temporal shift, eliminating the need for more complicated light filtering schemes. The system has been used to detect droplet populations containing four unique combinations of dyes and to detect sub-nanomolar concentrations of fluorescein.

Multicolor fluorescence detection in droplet microfluidics typically involves bulky and complex epifluorescence microscope-based detection systems. Here we describe a compact and modular multicolor detection scheme that utilizes an array of optical fibers to temporally encode multicolor data collected by a single photodetector.

Fluorescence assays are the most common readouts used in droplet microfluidics due to their bright signals and fast time response. Applications such as ...

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone

The ion concentration polarization (ICP) phenomenon is one of the most prevailing methods to preconcentrate low-abundance biological samples. The ICP induces a noninvasive region for charged biomolecules (i.e., the ion depletion zone), and targets can be preconcentrated on this region boundary. Despite the high preconcentration performances with ICP, it is difficult to find the operating conditions of non-propagating ion depletion zones. To overcome this narrow operating window, we recently developed a new platform for spatiotemporally fixed preconcentration. Unlike preceding methods that only use ion depletion, this platform also uses the opposite polarity of the ICP (i.e., ion enrichment) to stop the propagation of the ion depletion zone. By confronting the enrichment zone with the depletion zone, the two zones merge together and stop. In this paper, we describe a detailed experimental protocol to build this spatiotemporally defined ICP platform and characterize the preconcentration dynamics of the new platform by comparing them with those of the conventional device. Qualitative ion concentration profiles and current-time responses successfully capture the different dynamics between the merged ICP and the stand-alone ICP. In contrast to the conventional one that can fix the preconcentration location at only ~5 V, the new platform can produce a target-condensed plug at a specific location in the broad ranges of operating conditions: voltage (0.5-100 V), ionic strength (1-100 mM), and pH (3.7-10.3).

The protocol for a novel ion concentration polarization (ICP) platform that can stop the propagation of the ICP zone, regardless of the operating conditions is described. This unique ability of the platform lies in the use of merging ion depletion and enrichment, which are two polarities of the ICP phenomenon.

The ion concentration polarization (ICP) phenomenon is one of the most prevailing methods to preconcentrate low-abundance biological samples. The ICP ...