We acknowledge funding from the Chemical and Biological Metrology programme of the UK's National Measurement Office. We thank Sebastian van de Linde, Miklos Erdelyi and Eric Rees for technical advice and suggestions. We thank Miklos Erdelyi, Eric Rees and Max Ryadnov for helpful comments and discussions on this manuscript.

Note: Throughout this protocol, tips and suggestions are found following certain steps. The notation "*1" indicates that note 1 is relevant to this specific step, and so on.
1. Fluorescent Dextran Coating of Glass
<ol>
	<li>Add 200 &mu;l of 0.01% poly-L-lysine solution to each well of an 8-chamber coverglass and incubate for 10 min. Remove with a pipette to ensure that no is liquid remaining.</li>
	<li>Reconstitute dextran-Alexa 647*1 according to manufacturer's instructions to create a 2 mg/ml stock solution. From this, dilute 0.25 &mu;l into 25 &mu;l of de-ionized water to create a 20 &mu;g/ml solution.</li>
	<li>To create a high density coating of dextran-Alexa 647 solution dilute 20 &mu;l of the 20 &mu;g/ml solution into a total of 200 &mu;l of de-ionized water. For a medium density solution dilute 2 &mu;l in 200 &mu;l of de-ionized water (1:10,000 dilution from the original stock solution). For a low density solution dilute 0.2 &mu;l in 200 &mu;l of de-ionized water (1:100,000 dilution from the original stock solution).</li>
	<li>Add 200 &mu;l of the diluted dextran-Alexa 647 solutions to each well and incubate for 10 min. Longer incubation times can be used which may result in a denser dextran coating. Remove and wash with H2O three times*2</li>
</ol>
Note 1: Other dextran-dye conjugates can be used. Unconjugated dextran can also be conjugated to dyes if desired combinations are not commercially available.
Note 2: The same dextran chambers can be reimaged over a period of weeks although the uniformity of the fluorescence may decrease. Storage at 4 &deg;C in the absence of any buffer is recommended.
2. Fluorescent Actin Filaments on Glass
<ol>
	<li>Add 200 &mu;l of 0.01% poly-L-lysine solution to each well of the chamber and incubate for 10 min*3. Remove with a pipette to ensure that no liquid is remaining.</li>
	<li>Add 90 &mu;l of general actin buffer (reconstituted according to manufacturer's instructions) to each chamber. Add 10 &mu;l of 10 &mu;M preformed actin filament solution and 1 &mu;l phalloidin-Alexa 647 (0.2 units, when dissolved in 1.5 ml of methanol as per manufacturer's instructions) and gently pipette up and down to mix. Incubate for 30 min*4.</li>
</ol>
Note 3: Increasing the volume of the filament solution within the chamber results in fewer filaments binding to the poly-L-lysine coated glass.
Note 4: Incubation times of up to 48 hr at 4 &deg;C have been tested with good results. Actin filament image quality deteriorates once a chamber has been exposed to switching buffer so it is not recommended to use the same sample for more than one day.
3. Microsphere Fluorescent Beads as Fiducial Markers
<ol>
	<li>Dilute 1 &mu;l of TetraSpeck beads into 200 &mu;l PBS and mix.</li>
	<li>Add the diluted beads into an imaging chamber and wait for 15 min*5. Remove the solution and wash 3 times with PBS prior to imaging.</li>
</ol>
Note 5 - the dilution and incubation time can be adjusted to obtain different densities of beads. This protocol typically results in between 3 - 10 beads per 20.5 &mu;m x 20.5 &mu;m field-of-view.
4. Epidermal Growth Factor Cell Staining
<ol>
	<li>Culture HeLa cells in imaging chambers to approximately 80% confluency in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin solution.</li>
	<li>Remove the culture medium and wash with PBS. Then add 500 &mu;l of 4% formaldehyde solution (4 ml 10% formaldehyde solution, 1 ml 10X PBS, 5 ml water) for 10 min. Remove the formaldehyde and wash 3 times with PBS. Do not allow the cells to remain dry and always use PBS buffered solutions to avoid hypotonic stress.</li>
</ol>
CAUTION - formaldehyde is extremely toxic. Ensure that appropriate gloves, eye protection and lab coats are worn. Check local guidelines for disposal of formaldehyde.
<ol start="3">
	<li>Reconstitute EGF-Alexa 647 according to manufacturer's instructions to create a 50 &mu;g/ml stock solution. Add 2 &mu;l of this stock solution to 200 &mu;l of 0.1% BSA solution (in PBS). Remove the PBS from the cells, add the EGF solution and incubate for 30 min.</li>
	<li>Remove solution and wash 3 times with PBS before adding a blocking solution of 0.1% BSA (in PBS) for 15 min. Remove this and wash a further 3 times with PBS prior to imaging.</li>
</ol>
5. Switching Buffer Preparation
<ol>
	<li>Make an enzyme stock solution (A) with 10 &mu;l of catalase (20 &mu;g/ml), 20 &mu;l of 1 M Tris (2-carboxyelthyl) phosphine hydrochloride (4 mM), 2.5 ml glycerin (50%), 125 &mu;l of 1 M KCl (25 mM), 100 &mu;l of 1 M pH 7.5 Tris-HCl (20 mM), 5 mg of glucose oxidase (1 mg/ml) and top up to 5 ml volume with diH20. This is sufficient to make 100 x 50 &mu;l aliquots, which can be stored at -20 &deg;C and used for up to 1 year.</li>
	<li>) Make a glucose stock solution (B) with 4 g glucose (100 mg/ml), 4 ml glycerin (10%) and 36 ml diH20. This is sufficient to make 100 x 400 &mu;l aliquots, which can be stored at - 20 &deg;C and used for up to 1 year.</li>
	<li>Make a reducing agent stock solution (C) with 113.6 mg of MEA-HCl (1M) and 1 ml of diH20. Use fresh or make 10 x 100 &mu;l aliquots, which can be stored at -20 &deg;C and used for up to 1 month (do not refreeze aliquots).</li>
	<li>Just prior to imaging, mix the enzyme (A), glucose (B) and reducing agent (C) stock solutions together in the ratio 50 &mu;l, 400 &mu;l, 100 &mu;l and make up to 1 ml with PBS*6. This buffer will now scavenge oxygen and have a reducing environment (100 mM MEA-HCl)*7. The final pH should be in the range 6.0 - 8.5 (adjustment is not normally necessary)*8.</li>
</ol>
Note 6 - this buffer is suitable for use with carbocyanine-based dyes such as Cy5 and Alexa 647.
Note 7 - the final enzyme concentrations are 50 &mu;g/ml (5 unit/ml) of glucose oxidase and 1 &mu;g/ml (40-60 units/ml) of catalase. The enzymatic activity (units) is given by suppliers and can vary. The calculations for catalase assume that 1 &mu;g/ml final concentration after step 5.4 will contain 50 units of enzyme. Various buffer compositions including similar oxygen scavenging components can be found 21,30,40. For a summary of buffer and dye combinations see references 28,29. Glycerin and TCEP are required for long-term storage at -20 &deg;C.
Note 8 - if imaging actin filaments add 2 mM MgCl2 and 0.2 mM ATP to help stabilize the filaments.
6. Microscope Acquisition of STORM Data (using Alexa 647 dye)
<ol>
	<li>Switch on the STORM/PALM microscope, preferably at least 3 hr before imaging to allow a thermal equilibrium to be reached. Imaging before this has an increased chance of drift.</li>
	<li>Insert the imaging chamber into the microscope stage sample holder. Ensure that the sample is firmly in the holder and is flat.</li>
	<li>Remove the PBS from the imaging chamber and then fill to the top with the switching buffer. Carefully place a coverslip over the top of the chamber, making sure that there are no bubbles at all and that the entire chamber is covered. Top up with additional buffer or PBS if any bubbles are seen otherwise buffer performance can decline.</li>
</ol>
CAUTION - to minimize the chances of lateral and axial drift of the sample in relation to the objective lens it is recommended that the sample and the buffer are left to equilibrate to room temperature for at least 15 min prior to imaging.
<ol start="4">
	<li>Locate a fluorescent structure of interest to be imaged. Select the desired angle of illumination, in this case, a TIRF or highly inclined angle is recommended as this improves the signal-to-noise ratio by minimizing out-of-focus light, which is particularly of benefit for cell samples. Take a reference diffraction-limited image of the structure prior to STORM imaging.</li>
	<li>Increase the excitation laser (with an appropriate excitation wavelength of approximately 640 nm) to a high power, corresponding to approximately 2 kW/cm2 whilst imaging with camera settings of 10 msec exposure and a cycle time of approximately 50 Hz (frames per second). Once the fluorophores have transitioned into a sparse blinking pattern (probably within 10 sec for most samples) collect 10,000 frames*9.</li>
</ol>
Note 9 - 10,000 frames is suitable for the samples described here but it may be necessary to increase the frame number to 50,000 or more for other samples.
7. Reconstructing Super-Resolution Images from Raw Data (using rainSTORM)
<ol>
	<li>Open the rainSTORM.m file from within MATLAB and run (Figure 1A).</li>
	<li>In the rainSTORM window (Figure 1B) select the image file to be analyzed using the browse button. This should be a .tif file (ImageJ can be used to convert other file types into a tif format). Alter the pixel width to match the raw data of the microscope system used to acquire the data*10. Leave the other values to default.</li>
</ol>
Note 10 - A typical EMCCD camera has a pixel size of 16 &mu;m so on a system with a 100X objective lens the pixel size on the image will be 160 nm. On commercial systems the pixel size is usually displayed within the software. Pixel sizes vary between 100 nm and 160 nm for most localization microscopes.
<ol start="3">
	<li>Press the 'Process Images' button and wait until a preliminary image appears. The duration of the processing will depend on the file size, computer specification and the number of candidate blinks within the raw data*11.</li>
</ol>
Note 11 - 10,000 frame sequences of actin and EGF data took 23 sec and 25 sec to process respectively using a PC with an Intel Xeon E5420 CPU. Using the same computer without a parallel processing toolbox in MATLAB, or with a computer without multiple core processing, times were 66 sec and 81 sec respectively.
<ol start="4">
	<li>To generate an updated super-resolution image press the 'Open Reviewer' button and a second window will appear (Figure 1C). Press the 'Adjust Contrast' button in order to change the image display as desired (Figure 1D). In some cases, where the image is very dark the maximum value should be decreased.</li>
	<li>Use the reviewer window (Figure 1C) to generate useful image quality metrics and refine the super-resolution image further. Set the first three quality control parameters to values of 4,000, 0.1 and 0.8-2.0 respectively*12. Update the counts per photon value, which should either be based on a photon calibration measurement or using photon-curve calibration curve values specified by the camera manufacturer for a particular EM gain setting. This is critical for obtaining accurate precision and resolution measurements*13.</li>
</ol>
Note 12 - Signal Counts rejects blinks based on brightness criteria. The higher the value the brighter the blink must be to become accepted as a localization in the final image. This may need to be altered depending on the photon output of the dye and exposure time and sensitivity of the camera. Tolerance rejects blinks if there is significant square error between the signal and the fitted Gaussian i.e. double peaks. PSF Sigma Range rejects blinks if the fitted width of the PSF lies out of this range, i.e. a narrower range can be used to reject out-of-focus signals and large aggregated blobs of constant fluorescence. Using a wider range may result in mislocalization artifacts appearing in the final image. In practice, it is recommended to perform initial quality control using the localization precision cutoff parameter.
Note 13 - for more on resolution metrics see references 23,27. In brief by knowing the number of photons produced by each blink it is possible to calculate the localization precision of each localization and consequently derive overall mean precision estimates for the entire image. Using an Andor iXON DU-897E with a gain setting of 200 the Counts per Photon value is 9.04.
<ol start="6">
	<li>Alter the localization precision cutoff (Figure 1C) to tradeoff between optimizing mean localization precision against localization number in the final image. Values of 30-50 nm are recommended depending on the quality of the data and the sample. Both the histograms and the info.txt files can be used to inform this decision (Figures 1F and 1G).</li>
	<li>The reconstruction scale factor (Figure 1C) default is 5, which will generate super-resolution pixels of 32 nm assuming that the pixel width in the original images is 160 nm. If the raw images have a pixel size of 100 nm this will produce super-resolution images with pixels of 20 nm. Increase the scale factor to produce smaller super-resolution pixels in the final image*14.</li>
</ol>
Note 14- Resolution of localization microscopy depends on the smoothing required for visualization (ie. the pixel size of a simple histogram reconstruction) as well as the localization precision. In practice, the reconstruction pixel size should generally be smaller than the localization precision (see the Mean Precision Estimate metric in the info text file - steps 6.11 &amp; 6.12). In this case the loss of resolution due to reconstruction pixel size will be small 23,27. For example the mean precision estimates in the row and column direction of Figure 4E are 16.1 nm and 16.2 nm. A pixel size of 16 nm has been used to visualize this data (reconstruction scale factor of 10 with an original pixel width of 160 nm).
<ol start="8">
	<li>Modify the limit frame range (Figure 1C) to restrict the reconstruction to subsets of the raw data, for example [2001-inf] would exclude the initial 2,000 frames of raw data.</li>
	<li>Press the 'Run Reviewer' button (Figure 1C) to generate an updated super-resolution image (Figure 1E).</li>
	<li>Press the 'View Histograms' button (Figure 1C), in order to display image quality metrics (Figure 1F)*15.</li>
</ol>
Note 15 - The graph in the top right depicting the number of accepted localizations against camera frame number and the Thompson Localization Precisions histogram in the bottom right (Figure 1F) can be used to inform the localization precision cutoff review option. For example, using a 50 nm cutoff would exclude all the localizations with worse precision from being included in the final super-resolution image.
<ol start="11">
	<li>Press the 'Save Image' button in the reviewer (Figure 1C) in order to save all of this data*16.</li>
</ol>
Note 16 - Between 3 and 5 files can be saved depending on the options selected (sum image, STORMdataImage, STORMprocessed, info &amp; hists), see Figure 1G. The STORM processed image is displayed with modified contrast and color maps. The STORMdataImage is a grayscale image, in which the gray level of each pixel equals the number of localizations which were identified within it.
<ol start="12">
	<li>After examining the data (e.g. Info.txt file and histograms) return to step 7.6 and repeat the subsequent steps with different reviewer parameters if desired. Pressing 'Save Image' in step 7.11 will overwrite the previously saved data.</li>
</ol>
8. Box Tracking and Drift Correction (using rainSTORM)
<ol>
	<li>Follow steps 7.1 - 7.9 to generate an image in the normal way.</li>
	<li>Press the 'Box Tracking' button in the reviewer (Figure 1C) and click and drag a box over the fiducial marker or structure of interest on the reviewed image.</li>
	<li>Wait until a new image appears, which will display the 'Boxed Positions' (see Figures 6B, 6C and 6F for examples). Save this image if desired.</li>
	<li>If the object of interest is a fiducial marker then drift correction can be performed by clicking the 'Set Anchor' button followed by the 'Subtract Drift' button. Finally click 'Run Reviewer' again to generate a new STORM image, which will now have all localizations corrected according to the fiducial marker positions. The bead positions are deleted from the final reviewed image.</li>
	<li>If there are other fiducial markers within the final drift corrected image, these can be removed by pressing 'Box Tracking', 'Delete Boxed' and then 'Run Reviewer' as many times as desired.</li>
</ol>

We have nothing to disclose.

We show with some simple test samples and the freely-available processing software rainSTORM it is possible to optimize STORM super-resolution imaging. These tools and methods will provide useful starting points for new users and ways for experienced users to increase confidence in their microscopes and their use of them to study biological and cellular structures with unprecedented detail. By using a combination of samples with known or well-understood structures and an algorithm that can produce a number of useful image quality metrics, such as mean precision estimates, localization number and histograms showing it is possible to improve image quality and to have greater confidence in the STORM imaging process. There is no one-size fits all approach to acquiring the data as there are a number of different commercial and self-built microscope configurations that can be used. Moreover, there are many sample preparation and image acquisition steps which can influence the final image therefore having software tools and test samples is critical to understanding and optimizing STORM image quality.
In addition these protocols can provide useful and less ambiguous ways of troubleshooting any problems that may arise. For example the dextran sample is a very useful way to identify if there is any laser beam misalignment or uneven illumination of the sample. If there are concerns that the switching buffer may not be working a very simple visual test to see if there is any 'blinking' will help. Actin filaments are a useful way of measuring resolution using FWHM comparisons as well as highlighting drift and mislocalization artifacts. However, it should be noted that as localization-based super-resolution methods can be fluorophore density sensitive, notwithstanding the other contributing factors, such as exposure times, frame rates, laser powers and the way the image is processed, it is impossible to assign a resolution to a particular microscope and assume that all images will have that resolution. What is possible, however, is to measure various aspects of resolution such as mean localization precisions, localization number and drift 27. Even if fiducial markers cannot be incorporated into every experiment they can, at least, be used to characterize a microscope system, its environment and better understand operational considerations such as how much time is required to reach thermal equilibrium after start up. As well as correcting for lateral drift, fiducial markers can be used to characterize and correct for axial drift, although this requires the use of an astigmatic lens and a feedback mechanism to correct the sample position whilst the images are being acquired 43. Commercial super-resolution systems will usually include some sort of stability control or focus-lock mechanism, which may be a more practical solution for correcting focus drift.
There are alternatives to non-specifically coating the glass with dextran, such as using dyes directly or other conjugate molecules, such as secondary antibodies. A limitation of these approaches is that the number of molecules bound to the glass is not known. Alternative filamentous structures that have been used include microtubules 28 and DNA21. However, the combination of very small size and convenient commercially available reagents make actin an attractive alternative, particularly as the separation distance of diverging or branched filaments can also be a useful measurement of system performance 27.
There is room for further development of test samples, despite recent progress in this area 28,29,46,47. In particular, multi-color imaging presents a number of challenges in all 3 main aspects of the imaging, sample labeling, image acquisition (hardware), and software (image processing and alignment). There have a been a number of publications addressing these aspects 4-6 and it is therefore clear that appropriate test samples and methodologies are critical to generating and reliably interpreting these types of images. Indeed, recently it was shown that dSTORM could be used to take two color images of, and resolve, the highly symmetrical nature of the nuclear pore complex and the authors suggested that this would be an ideal way to assess performance of chromatic aberration corrections 45. Another interesting approach is the use of DNA origami to create a nanoruler, which creates the possibility of positioning fluorophores at specific sub-diffraction distances apart 46. This provides a way of assessing resolution and making distance measurements. However, the ultimate aim is to apply these super-resolution techniques to non-idealized samples, such as cells, which are complex three dimensional structures. In this case, a combination of more thorough understanding of the technique combined with software tools that aid the user in acquiring data, processing it in appropriate ways, and providing image metrics is likely to be the ultimate answer. 28,29,47,48

Recently a range of optical microscopy techniques have been developed, typically referred to as super-resolution microscopy or nanoscopy, which can bypass the diffraction limit and generate images with resolutions of 100 nm or better 1,2 . Since the announcement of super-resolution microscopy as being the Nature Methods method of the year in 2008, there has been a great deal of development of localization-based microscopes. For example, there are multi-color applications 3-6 , 3D implementations 7-12, and even live cell applications 5,13-17 . Moreover, as these systems are being commercialized and are now making their way out of optics laboratories into the hands of cell biologists there is likely to be a further increase in their use and application to biomedical questions.
One branch of this family is the localization-based methods which work by building up an image molecule-by-molecule. In order to do this, the majority of fluorescent molecules within the sample must be switched off so that only a few spatially-separated molecules are active at any one time. These molecules are then rapidly switched on and off and many images are taken so that a significant part of the population is imaged to reflect the underlying structure with sub-diffraction precision. A number of approaches have been published including GSDIM 18, PALM 19 , fPALM 20 , STORM 21 and RESOLFT 22. Algorithms that measure the position of a single molecule detection can then be used to locate the actual position of the molecule with precisions better than 20 nm using Gaussian fitting23, for example rapidSTORM 24,25 QuickPALM 26, palm3d 12 and rainSTORM27. When imaging cell or other biological samples, which have a high molecule density, it is therefore necessary to take many thousands of frames of this blinking, spatially separated, signal in order to image a significant proportion of the labeled molecules.
Stochastic optical reconstruction microscopy (STORM) and the highly related dSTORM and GSDIM methods are localization-based super-resolution methods, which have been demonstrated to work with commercially available organic dyes 21. They have since been shown to be applicable to a number of different dyes 28-30, which makes the methodology particularly attractive because of the specificity and relative convenience of well-established immunolabeling approaches to perform fluorescence microscopy. Consequently, there is easy access to a range of dye-antibody and dye-biomolecule conjugates, which have the potential to be used in localization-based super-resolution imaging. Whilst the general principles of STORM and similar approaches are relatively simple, and at first sight the hardware and sample preparation seem relatively straightforward, there are a number of steps in the process which are critical to achieving high quality, artifact-free, super-resolution images.
As with all microscopy techniques the process can be thought of in 3 main steps: first, sample preparation, second, image acquisition and, third, image processing and/or image analysis and interpretation. The additional resolving power and method of generating super-resolution images using a localization-based approach introduces some new problems and considerations 31-33. Starting with sample preparation, when performing immunolabeling, particularly indirect immunofluorescence where a primary and secondary antibody combination is used, it should be noted that the fluorescent dye may be up to 20 nm away from the molecule of interest. In the case of microtubules, this results in diameters of 35-50 nm compared with an expected microtubule diameter of 25 nm 28,30 . Also, the labeling density should meet the Nyquist criteria in order to generate a high quality image 14. For example for an anticipated image resolution of 20 nm along a filamentous structure there should be a dye molecule at least every 10 nm 27. Whilst many dyes have been published to work for localization-based approaches the overall performance of the dye is a mix of at least four important criteria, namely detected photons per switching event (the brightness of each blink - brighter is better), the equilibrium on-off duty cycle (the contrast ratio of dyes in the off versus on state - more off is generally better), the survival fraction (a low bleaching rate is better) and the number of switching cycles (the number of blinks per fluorophore - more is better for high resolution, although 1 blink per fluorophore can be an advantage for molecule counting purposes). The situation is further complicated by the fact that these properties for any given dye can vary in different buffer conditions and with laser power 28,29 . In addition, as well as these unique STORM considerations, image quality can be improved by optimizing sample preparation in the same way as more traditional fluorescence microscopy techniques for example by minimizing autofluorescence by modification of fixation conditions and the use of quenching reagents. Also, minimizing non-specifically bound fluorophores is important, which can be done by adjusting label concentrations, incubation times and blocking and washing steps.
The second step of image acquisition is also critical. The optimum settings on the microscope will depend on the dye, buffer conditions, labeling density, and sample type, e.g. monolayers on glass, cells or tissue samples. The main considerations are camera exposure time, frame number, illumination angle (TIRF, HILO, Epi) and laser power. The aim is to collect as many bright spatially separated blinks as quickly as possible. If the background is very high or the blinks are not very bright, in other words the signal-to-noise ratio is poor, the reconstruction algorithm will not be able to localize the positions as accurately. As well as maximizing the localization precision, i.e. the accuracy with each molecule position can be measured, image quality also depends on a high number of localizations. If an insufficient number of the molecules of interest are imaged, either due to poor labeling efficiency, excessive photobleaching or an inadequate frame number, then the resulting super-resolution image will be punctate and discontinuous as Nyquist criteria will not have been met 14,27.
And finally, the third step, image processing, is particularly important compared with standard fluorescence microscopy techniques. There is a range of freely and commercially available algorithms, which is both an advantage, in terms of choice, and a disadvantage, in that it can be confusing to know which is most appropriate to use. If for example the raw data has well-spaced spatially distinct blinks then a single-molecule fitting algorithm can be highly accurate and efficient, for example by the sparse fitting algorithms available in rainSTORM 27, rapidSTORM 24,25 , palm3d 12 and QuickPALM 26software. If the raw data contains a lot of overlapping signals then algorithms which may be more appropriate include DAOSTORM 34, 3B 35 and deconSTORM 36. Moreover, these algorithms contain thresholds for various criteria such as signal counts, or photons per blink, as well as various different image display options such as visualizing with smoothed Gaussian functions or as histograms with pixel grids, where the super-resolution pixel size can be selected by the user. All of these options change the appearance of the final image and have implications for image interpretation and analysis.
Therefore, we present 3 test samples which will provide the new user with a starting point for dye-based localization-based super-resolution experiments, which for the sake of clarity we will refer to as STORM, and more experienced users the opportunity to further optimize their experiments. First, it is possible to coat the surface of glass with a fluorescent layer of dextran-dye conjugate. This provides a quick and simple way to establish that the microscope, dye and buffer are working to generate blinking fluorescent signal. The method can then be extended by comparing mean localization precision and number metrics generated by rainSTORM to optimize buffer conditions, image acquisition settings and test different dyes. Second, we present a simple protocol for preparing actin filaments on glass which can be readily labeled using phalloidin-dye conjugates. These provide ideal structures to take measurements of resolution 27 and typically the full width half maximum (FWHM) of a filament is given as an empirical estimate of resolution 37. It should be noted that resolution varies between samples and between images within the same sample because resolution in localization-based super-resolution microscopy is a function of fluorophore brightness, background noise and localization density 27 and these are not necessarily constant throughout the specimen. Actin filaments are used to demonstrate potential artifacts such as mislocalizations and drift and how they can be identified with software features within rainSTORM. Moreover, we describe the use of fluorescent fiducial markers to both measure and correct drift. And third, the staining of cells with epidermal growth factor (EGF)-dye conjugates is described. EGF provides a useful indicator of super-resolution image performance, because a proportion of the receptor at the cell surface undergoes endocytosis via vesicles, which are sub-diffraction sized structures of approximately 50-150 nm in diameter 27,38,39 .

<table border="1">
	<tbody>
		<tr>
			<td>Name of Reagent/Material</td>
			<td>Company</td>
			<td>Catalog Number</td>
			<td>Comments</td>
		</tr>
		<tr>
			<td>Labtek Imaging chamberglass</td>
			<td>Fisher</td>
			<td>CBR-166-390E</td>
			<td>Sample preparation</td>
		</tr>
		<tr>
			<td>Inverted Microscope</td>
			<td>Olympus</td>
			<td>IX71</td>
			<td>* See below for alternatives</td>
		</tr>
		<tr>
			<td>100 X TIRF Objective Lens</td>
			<td>Olympus</td>
			<td>UAPON 100XOTIRF</td>
			<td>* See below for alternatives</td>
		</tr>
		<tr>
			<td>EMCCD Camera</td>
			<td>Andor</td>
			<td>iXon 897</td>
			<td>* See below for alternatives</td>
		</tr>
		<tr>
			<td>640 nm laser</td>
			<td>Toptica</td>
			<td>iBEAM-SMART-640-S</td>
			<td>*150 mW - for imaging Alexa 647 or Cy5 dyes</td>
		</tr>
		<tr>
			<td>LabVIEW</td>
			<td>National Instruments</td>
			<td>&nbsp;</td>
			<td>*Acquisition software (controlling hardware)</td>
		</tr>
		<tr>
			<td>PC</td>
			<td>Dell</td>
			<td>&nbsp;</td>
			<td>Windows XP (64 bit), Intel Xeon E5420 CPU, 16 GB RAM *Instrument control and image processing</td>
		</tr>
		<tr>
			<td>ImageJ</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Image analysis and processing <a href="http://rsbweb.nih.gov/ij" target="_blank">http://rsbweb.nih.gov/ij</a></td>
		</tr>
		<tr>
			<td>rainSTORM</td>
			<td>Laser Analytics Group (Cambridge) software</td>
			<td>&nbsp;</td>
			<td><a href="http://laser.cheng.cam.ac.uk/wiki/index.php/Resources" target="_blank">http://laser.cheng.cam.ac.uk/wiki/index.php/Resources</a></td>
		</tr>
		<tr>
			<td>MATLAB</td>
			<td>Running rainSTORM</td>
			<td>&nbsp;</td>
			<td><a href="http://www.mathworks.co.uk/products/matlab/" target="_blank">http://www.mathworks.co.uk/products/matlab/</a></td>
		</tr>
		<tr>
			<td>*Example of self-built STORM/PALM microscopes</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Also see reference 29 <a href="http://code.google.com/p/quickpalm/wiki/Tutorial_CustomMicroscope" target="_blank">http://code.google.com/p/quickpalm/wiki/Tutorial_CustomMicroscope</a></td>
		</tr>
		<tr>
			<td>*Commercial STORM/PALM super-resolution microscopes</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Leica SR GSD, Nikon N-STORM, Vutara SR-200, Zeiss Elyra P.1, DeltaVision OMX Blaze (Monet Localization) Alternatives to self-built microscopes</td>
		</tr>
		<tr>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Table 1. Materials &amp; Equipment</td>
		</tr>
		<tr>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>[header]</td>
		</tr>
		<tr>
			<td>PBS (10X)</td>
			<td>Fisher</td>
			<td>VX70013065</td>
			<td>1; 2; 3; 4</td>
		</tr>
		<tr>
			<td>Poly-L-Lysine</td>
			<td>Sigma</td>
			<td>P4707</td>
			<td>1.1; 2.1</td>
		</tr>
		<tr>
			<td>Dextran-Alexa fluor 647</td>
			<td>Invitrogen</td>
			<td>D-22914</td>
			<td>1.2</td>
		</tr>
		<tr>
			<td>General actin buffer</td>
			<td>Cytoskeleton Inc</td>
			<td>BSA01</td>
			<td>2.2</td>
		</tr>
		<tr>
			<td>Preformed-actin filaments</td>
			<td>Cytoskeleton Inc</td>
			<td>AKF99</td>
			<td>2.2</td>
		</tr>
		<tr>
			<td>Phallodin-Alexa fluor 647</td>
			<td>Invitrogen</td>
			<td>A22287</td>
			<td>2.2</td>
		</tr>
		<tr>
			<td>TetraSpeck Microspheres (0.1 micron)</td>
			<td>Invitrogen</td>
			<td>T-7279</td>
			<td>3.1</td>
		</tr>
		<tr>
			<td>HeLa cells</td>
			<td>ATCC</td>
			<td>CCL-2</td>
			<td>4.1</td>
		</tr>
		<tr>
			<td>DMEM</td>
			<td>Fisher</td>
			<td>VX31966021</td>
			<td>4.1</td>
		</tr>
		<tr>
			<td>FBS</td>
			<td>Fisher</td>
			<td>VX10500064</td>
			<td>4.1</td>
		</tr>
		<tr>
			<td>Pen/Step</td>
			<td>Invitrogen</td>
			<td>15070063</td>
			<td>4.1</td>
		</tr>
		<tr>
			<td>Plastic dishes</td>
			<td>Invitrogen</td>
			<td>734-0006</td>
			<td>4.1</td>
		</tr>
		<tr>
			<td>EGF - Alexa fluor 647</td>
			<td>Invitrogen</td>
			<td>E35351</td>
			<td>4.3</td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>Sigma</td>
			<td>A7906</td>
			<td>4.3, 4.4</td>
		</tr>
		<tr>
			<td>Formaldehyde - 10% solution EM grade</td>
			<td>Polysciences</td>
			<td>04018-1</td>
			<td>4.2</td>
		</tr>
		<tr>
			<td>Catalase</td>
			<td>Sigma</td>
			<td>C100</td>
			<td>5.1</td>
		</tr>
		<tr>
			<td>Glucose oxidase</td>
			<td>Sigma</td>
			<td>G2133</td>
			<td>5.1</td>
		</tr>
		<tr>
			<td>KCl</td>
			<td>Sigma</td>
			<td>P9541</td>
			<td>5.1</td>
		</tr>
		<tr>
			<td>TCEP</td>
			<td>Sigma</td>
			<td>C4706</td>
			<td>5.1</td>
		</tr>
		<tr>
			<td>Tris</td>
			<td>Sigma</td>
			<td>93352</td>
			<td>5.1</td>
		</tr>
		<tr>
			<td>Glucose</td>
			<td>Sigma</td>
			<td>C7528</td>
			<td>5.2</td>
		</tr>
		<tr>
			<td>MEA-HCl</td>
			<td>Sigma</td>
			<td>M6500</td>
			<td>5.3</td>
		</tr>
		<tr>
			<td>Glycerin</td>
			<td>Sigma</td>
			<td>G2289</td>
			<td>5.1; 5.2</td>
		</tr>
		<tr>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>&nbsp;</td>
			<td>Table 2. Reagents</td>
		</tr>
	</tbody>
</table>

test samples for optimizing storm super-resolution microscopy

STORM is a recently developed super-resolution microscopy technique with up to 10 times better resolution than standard fluorescence microscopy techniques. However, as the image is acquired in a very different way than normal, by building up an image molecule-by-molecule, there are some significant challenges for users in trying to optimize their image acquisition. In order to aid this process and gain more insight into how STORM works we present the preparation of 3 test samples and the methodology of acquiring and processing STORM super-resolution images with typical resolutions of between 30-50 nm. By combining the test samples with the use of the freely available rainSTORM processing software it is possible to obtain a great deal of information about image quality and resolution. Using these metrics it is then possible to optimize the imaging procedure from the optics, to sample preparation, dye choice, buffer conditions, and image acquisition settings. We also show examples of some common problems that result in poor image quality, such as lateral drift, where the sample moves during image acquisition and density related problems resulting in the 'mislocalization' phenomenon.

Watch this Scientific Journal Video about Test Samples for Optimizing STORM Super-Resolution Microscopy at JoVE.com

Test Samples for Optimizing STORM Super-Resolution Microscopy

We describe the preparation of three test samples and how they can be used to optimize and assess the performance of STORM microscopes. Using these examples we show how to acquire raw data and then process it to acquire super-resolution images in cells of approximately 30-50 nm resolution.

STORM is a recently developed super-resolution microscopy technique with up to 10 times better resolution than standard fluorescence microscopy ...

test-samples-for-optimizing-storm-super-resolution-microscopy

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JoVE Journal

Biology

30.9K Views.  National Physical Laboratory. We describe the preparation of three test samples and how they can be used to optimize and assess the performance of STORM microscopes. Using these examples we show how to acquire raw data and then process it to acquire super-resolution images in cells of approximately 30-50 nm resolution.