Name: Preparation and Observation of Thick Biological Samples by Scanning Transmission Electron Tomography (Video) | JoVE Journal
Uploaded: 2017-03-12T13:00:00.000+00:00
Duration: 8 min 4 s
Description: Learn scanning transmission electron tomography for structural biology using convergent beam imaging of thick biological specimens. This method enables three-dimensional reconstruction with depth of field recovery for detailed analysis.

ai_agent_IP

ai_agent

maintenance

instantTrialDurationMinutes

isBiopharma

enableNewMyJoveSectionDesign

educationFeatures

seoMetaApi

ai_copilot_institution_blacklist

ai_chat_institution_blacklist

freeAccessWindow

ssoRoleCapture

scheduledMaintenanceBanner

joveLabsFeatures

disable_autoplay_for_bots

extended_trial_duration

5 minutes

This work was funded by two ANR grants (ANR-11-BSV8-016 and ANR-10-IDEX-0001-02). We also acknowledge the PICT-IBiSA for providing access to chemical imaging equipment.

Caution: Consult the material safety data sheets (MSDSs) of the various reagents before using them. Several of the chemicals used during sample preparation are toxic, carcinogenic, mutagenic, and/or reprotoxic. Use personal protective equipment (gloves, lab coat, full-length pants, and closed-toe shoes) and work under a fume hood while handling the sample. Sectioning the sample with an ultramicrotome involves the use of sharp instruments, and careful use of these tools is mandatory. In the steps described below, the authors assume that the sample is a cell culture sample. The protocol may need to be modified according to the sample type, especially the centrifugation steps.
1. Preparation of Buffers and Mixtures
<ol>
	<li>Prepare phosphate-buffered saline (PBS) solution (137 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, and 1.76 mM KH2PO4).</li>
	<li>Prepare solutions containing 30%, 50%, and 70% ethanol in PBS for sample dehydration. Perform sample dehydration by gradually incubating the sample in increasing ethanol concentrations.</li>
	<li>Prepare epoxy resin by mixing bisphenol-A-(epichlorohydrin) (20 mL), dodecenyl succinic anhydride (9 mL), methyl-5-norbornene-2,3-dicarboxylic (11 mL), and 2,4,6-tris(dimethylaminomethyl)phenol (0.7 mL); other mixing ratios can be used depending on the desired hardness of the resin.</li>
	<li>Prepare solutions containing 30%, 50%, and 70% epoxy resin in ethanol for sample embedding. Perform resin embedding by gradually incubating the sample with increasing resin concentrations. 
	NOTE: The volumes of the prepared solutions depend on the type of sample that is studied. More solutions are needed for tissues than for cell cultures.</li>
</ol>
2. Fixation and Coloration of the Sample
<ol>
	<li>Centrifuge the cell culture for 5 min at 5,000 x g. Perform all of the following centrifugations using the same conditions.</li>
	<li>Discard the supernatant and fix the cell pellet by resuspending it in PBS (1 mL) with 4% paraformaldehyde and 2% glutaraldehyde. Incubate it at room temperature for 30 min (Figure 1A). Alternatively, fix the cells at 4 °C overnight or over the weekend.</li>
	<li>After centrifugation, remove the supernatant and wash the pellet 3 times with PBS (1 mL) to completely remove the fixative agents.</li>
	<li>Post-fix the sample with 1% OsO4 in PBS (1 mL) for 30 min at room temperature.</li>
	<li>After centrifugation, remove the supernatant and wash the pellet 3 times with PBS (1 mL) to completely remove the OsO4. Deactivate the OsO4 in oil and discard.</li>
	<li>Add 2% uranyl acetate in PBS (1 mL) as a contrast agent and incubate the sample for 30 min at room temperature (Figure 1B).</li>
	<li>After centrifugation, remove the supernatant and wash the pellet 3 times with PBS (1 mL) to remove the unbound uranyl acetate; uranyl acetate contains radioactive elements and should be disposed of in a bin dedicated to radioactive waste. 
	NOTE: The incubation times can be modified according to the size of the sample. For example, fixation and staining of thicker samples, such as tissues samples, require longer incubation times. Longer incubation times may also be better for the dehydration and the embedding steps. Uranyl acetate can be replaced by a "uranyl-less" solution that contains Gadolinium salts.</li>
</ol>
3. Sample Dehydration
<ol>
	<li>After centrifugation, discard the supernatant and incubate the sample for 30 min at 4 °C in PBS (1 mL) with 30% ethanol (Figure 1C).</li>
	<li>Repeat step 3.1 using solutions with gradually increasing ethanol concentrations (50%, 70%, and up to 100%). During these dehydration steps, maintain the sample at 4 °C for sample preservation purposes.</li>
	<li>After centrifugation, discard the supernatant and resuspend the pellet in pure ethanol (1 mL); incubate overnight at 4 °C.</li>
</ol>
4. Resin Embedding
<ol>
	<li>After centrifugation, discard the supernatant and resuspend the pellet in ethanol with 30% epoxy resin (1 mL) for 30 min at RT (Figure 1D).</li>
	<li>Repeat step 4.1 using solutions with gradually increasing epoxy resin concentrations (50%, 70%, and up to 100%).</li>
	<li>After centrifugation, discard the supernatant and resuspend the pellet in pure epoxy resin (1 mL); incubate overnight at RT. The presence of hardening DMP-30 might trigger the polymerization of the resin; if this happens, prepare two batches of epoxy resin, one with and one without DMP-30.</li>
	<li>After centrifugation, resuspend the pellet in 200 µL of pure epoxy resin (containing the hardener) in a plastic capsule; the sample should be at the bottom of the plastic capsule.</li>
</ol>
5. Resin Polymerization
<ol>
	<li>Incubate the plastic capsule containing the sample in an incubator set at 60 °C for 48 h; other kinds of resin might polymerize with different settings.</li>
	<li>Remove the capsule from the incubator and verify that the resin has polymerized; the resin should be hard if pressed against a hard surface.</li>
	<li>Add pure epoxy resin (containing the hardener) on top of the polymerized resin containing the sample; this extra layer of resin will make it easier to cut the sample. Incubate the capsule at 60 °C for 48 h.</li>
</ol>
6. Sample Sectioning
<ol>
	<li>Mount the sample upside-down in a specimen holder so that the sample is towards the top and fix it on the trimming block of the ultramicrotome. Tightly lock the lever to secure the trimming block to the ultramicrotome.</li>
	<li>Using a razor blade or a similar sharp cutting instrument, cut out the plastic capsule to separate it from the polymerized resin. Cut the resin so that the sample is contained in resin in roughly the shape of a pyramid. There is no need to remove the entire plastic capsule; only remove the part covering the polymerized sample.</li>
	<li>Take the capsule and the specimen holder off of the trimming block and install them on the moving arm of the ultramicrotome.</li>
	<li>Install a trimming knife on the knife block and accurately trim the faces of the pyramid. The use of binoculars is advised to give a perfect shape to the pyramid; the better the pyramid, the better the sections will be.</li>
	<li>Take off the trimming knife and replace it with a histology knife that can be used to cut sections that are thicker than 0.5 µm.</li>
	<li>After filling the cuvette of the histology knife with the correct amount of water, bring the cutting edge of the knife to the surface of the sample and use the binoculars to adjust the capsule pitch angle so that the knife will slice perpendicularly to the pyramid.</li>
	<li>Adjust the cutting speed according to the desired section thickness to recover homogeneous sections.</li>
	<li>Let the section float over the water and fish it with a loop.</li>
	<li>Move the loop towards an electron microscopy copper grid that has been placed on top of filter paper. 
	NOTE: The grid should have been treated previously to increase its hydrophilicity. This can be performed with a grid-coating pen.</li>
	<li>Due to water absorption by the filter paper, let the section stick to the grid. Let it dry for few minutes before inserting it into the electron microscope.</li>
</ol>
7. Design of the Through-focal Tilt-series
<ol>
	<li>Collect through-focal images at constant focus intervals. 
	NOTE: The through-focal tilt-series consist of a set of through-focal images that are collected at each tilt angle of the tilt-series. The whole focus amplitude should be sufficient to cover the whole sample thickness.</li>
	<li>Determine the value of the focus interval. If the interval is equal to the depth-of-field, collect the entire sample in focus; this setting represents the highest sampling possible. If the interval is greater than the depth-of-field, some parts of the sample will not be acquired in focus, meaning that some parts of the sample will not be collected in focus.</li>
	<li>Calculate the depth-of-field of an electron beam from the electron's wavelength and the convergence semi-angle of the electron beam. Whereas the wavelength of electrons is directly linked to the acceleration voltage, use the convergence semi-angle provided by the electron microscope manufacturer or determine it experimentally from the diffraction pattern of a known specimen16. Because electrons accelerated at a wavelength λ hit the sample with a convergence semi-angle of α in an electron microscope, use the following equation to determine the depth-of-field (DOF): 
	 
	<img alt="Depth of Field (DOF) equation, optics formula, describes DOF calculation in optical systems." src="/files/ftp_upload/55215/55215eq1.jpg" data-altupdatedat="1788250015000" data-alt="Equation"></li>
	<li>Design the focal series so that the whole focus amplitude will cover the sample at its maximal apparent thickness (i.e., at its highest tilt). 
	NOTE: A 0.75 µm-thick sample will have an apparent thickness of 2.19 µm at a 70° tilt, so the focus amplitude should be greater than 2.19 µm. For this sample, if the focus interval determined above is equal to 50 nm, it will require 44 images (2.19 µm/50 nm) to cover the sample at its maximum apparent thickness. The whole focus amplitude is equal to the value of the focus interval multiplied by the number of focal steps. At the highest tilt (θ), the sample apparent thickness is defined as the following: 
	 
	<img alt="Sample thickness formula, diagram; describes relation with angle θ in material science." src="/files/ftp_upload/55215/55215eq2.jpg" data-altupdatedat="1788250015000" data-alt="Equation"></li>
</ol>
8. Sample Imaging
NOTE: It is beyond the scope of this protocol to describe how to set up an electron microscope in STEM mode; most of this information can be found in the reference manual provided by the electron microscope manufacturer. However, note the following: i) the spot size should be chosen according to the desired magnification; ii) the Ronchigram must be well-aligned; and iii) in BF mode, the camera length must be adjusted to select unscattered electrons while maintaining good illumination of the detector. Resin sections deposited on electron microscopy copper grids should be illuminated before image acquisition to prevent shrinkage. Resin shrinkage and charging effects might be confounded during image acquisition. The use of an objective lens aperture might improve sample stability when charging effects occur. However, in the specific case of STEM setups, the objective aperture is not compatible with HAADF imaging mode, and very small objective apertures are not compatible with BF imaging mode.
<ol>
	<li>Using low magnification (around 20,000X in STEM), browse through the sample and locate the region of interest.</li>
	<li>Adjust the eucentric height (Z-axis) so that the region of interest does not drift away while rotating the sample.</li>
	<li>Verify that the object of interest will remain visible throughout the entire tilt range.</li>
	<li>Because of the substantial number of images acquired during a through-focal tilt-series, use an automatic collection software. Either use a commercial solution or design a custom data collection software if desired. Ensure that the software program is able to perform the three following steps:
	<ol>
		<li>Track and focus as in a standard tilt-series collection scheme.</li>
		<li>Ensure that the through-focal images overlap with the Z-position of the sample.</li>
		<li>Automatically acquire a series of through-focal images at each tilt angle.</li>
	</ol>
	</li>
	<li>Give the software program the main parameters of the through-focal tilt-series (i.e., focal intervals, focal step, minimum tilt angle, maximum tilt angle, tilt step, and scanning speed).</li>
	<li>Start the image collection process and wait for the software program to finish.</li>
</ol>
9. Image Processing
NOTE: In this protocol, the through-focal tilt-series processing is performed using ImageJ plugins17. Supplementary Data 1 shows an ImageJ macro for the alignment step (Turboreg) and for merging in-focus information (Extended Depth of Field) for a through-focal tilt-series designed with three focus values.
<ol>
	<li>Align the images collected at the same tilt angle (i.e., the through-focal images). Since images do not have the same in-focus information, they do not harbor the same features for alignment; perform alignment by aligning neighboring images two by two (i.e., following a pyramidal hierarchy, with the closest focus values first) using Turboreg18, an ImageJ plugin.</li>
	<li>Consistently verify the alignment of the through-focal images at each tilt angle. Stack the aligned through-focal images to improve visual inspection. 
	NOTE: Only the zone that is in focus should move while browsing through the stack. Accurate alignment is the most important thing, since the following step consists of the recovery of the information that is in focus from different images.</li>
	<li>Merge the information that is in focus using Extended Depth of Field19, an ImageJ plugin; this will eventually generate a single image from the stack of images. Several settings can be used during the depth-of-field recovery, but use the highest settings to preserve the image information. 
	NOTE: The tilt-series is now composed of a single image per tilt angle, each image containing the in-focus information recovered from the through-focal images.</li>
	<li>Process the data. 
	NOTE: Standard tools for alignment and reconstruction can be used since the data has now been reduced to a standard tilt-series. In this protocol, TomoJ is used for data alignment and data reconstruction20,21. More details about how to use TomoJ can be found in the original publication22.</li>
	<li>Perform fine alignment of the tilt-series. 
	NOTE: A good strategy is to use gold beads as fiducial markers to accurately track shifts between images. Local minima can also be used if gold beads cannot be added to the sample.</li>
	<li>Perform a 3D reconstruction of the aligned data; several algorithms are available for performing the reconstructions in real space or Fourier space, each with advantages and limitations.</li>
	<li>If the final alignment of the tilt-series is poor, make some improvements by optimizing the initial steps. Reiterate the alignment steps if the final 3D reconstruction appears blurred or deformed; in practice, the greater the number of collected focal planes, the better the contrast and details of the 3D reconstruction. 
	NOTE: Several software programs can be used to process the through-focal tilt-series. However, the tools used in this protocol were chosen because, in our experience, they performed the best. Turboreg18 performed better in terms of aligning the images when a gradient of focus was present. More information can be found on the dedicated website23. The Extended Depth of Field plugin19 performed very well in terms of recovering the in-focus information from different images, whereas other tools resulted in visible pixels modifications. More information, especially regarding script writing, can be found on this dedicated website24.</li>
</ol>

<ol><li>De Rosier, D. J., Klug, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Reconstruction+of+three+dimensional+structures+from+electron+micrographs%5BTitle%5D)+AND+%22Nature%22%5BJournal%5D)">Reconstruction of three dimensional structures from electron micrographs.</a> Nature. 217 (5124), 130-134 (1968).</li>
<li>Gan, L., Jensen, G. J. <a target="_blank" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491709/">Electron tomography of cells.</a> Q Rev Biophys. 45 (1), 27-56 (2012).</li>
<li>Lucic, V., Rigort, A., Baumeister, W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Cryo-electron+tomography%3A+the+challenge+of+doing+structural+biology+in+situ%5BTitle%5D)+AND+%22J+Cell+Biol%22%5BJournal%5D)">Cryo-electron tomography: the challenge of doing structural biology in situ.</a> J Cell Biol. 202 (3), 407-419 (2013).</li>
<li>Al-Amoudi, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Cryo-electron+microscopy+of+vitreous+sections%5BTitle%5D)+AND+%22EMBO+J%22%5BJournal%5D)">Cryo-electron microscopy of vitreous sections.</a> EMBO J. 23 (18), 3583-3588 (2004).</li>
<li>Koguchi, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Three-dimensional+STEM+for+observing+nanostructures%5BTitle%5D)+AND+%22J+Electron+Microsc+%28Tokyo%29%22%5BJournal%5D)">Three-dimensional STEM for observing nanostructures.</a> J Electron Microsc (Tokyo). 50 (3), 235-241 (2001).</li>
<li>Midgley, P. A., Weyland, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((3D+electron+microscopy+in+the+physical+sciences%3A+the+development+of+Z-contrast+and+EFTEM+tomography%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">3D electron microscopy in the physical sciences: the development of Z-contrast and EFTEM tomography.</a> Ultramicroscopy. 96 (3-4), 413-431 (2003).</li>
<li>Sousa, A. A., Azari, A. A., Zhang, G., Leapman, R. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Dual-axis+electron+tomography+of+biological+specimens%3A+Extending+the+limits+of+specimen+thickness+with+bright-field+STEM+imaging%5BTitle%5D)+AND+%22J+Struct+Biol%22%5BJournal%5D)">Dual-axis electron tomography of biological specimens: Extending the limits of specimen thickness with bright-field STEM imaging.</a> J Struct Biol. 174 (1), 107-114 (2011).</li>
<li>Sousa, A. A., Leapman, R. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Development+and+application+of+STEM+for+the+biological+sciences%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">Development and application of STEM for the biological sciences.</a> Ultramicroscopy. , 38-49 (2012).</li>
<li>Ercius, P., Muller, D. <a target="_blank" href="https://www.researchgate.net/publication/239633484_Incoherent_Bright_Field_STEM_for_Imaging_and_Tomography_of_Ultra-Thick_TEM_Cross-sections">Incoherent bright field STEM for imaging and tomography of ultra-thick TEM cross-sections.</a> Microsc Microanal. 15, (2009).</li>
<li>Hyun, J. K., Ercius, P., Muller, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Beam+spreading+and+spatial+resolution+in+thick+organic+specimens%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">Beam spreading and spatial resolution in thick organic specimens.</a> Ultramicroscopy. 109 (1), 1-7 (2008).</li>
<li>Aoyama, K., Takagi, T., Hirase, A., Miyazawa, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((STEM+tomography+for+thick+biological+specimens%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">STEM tomography for thick biological specimens.</a> Ultramicroscopy. 109 (1), 70-80 (2008).</li>
<li>Biskupek, J., Leschner, J., Walther, P., Kaiser, U. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Optimization+of+STEM+tomography+acquisition--a+comparison+of+convergent+beam+and+parallel+beam+STEM+tomography%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">Optimization of STEM tomography acquisition--a comparison of convergent beam and parallel beam STEM tomography.</a> Ultramicroscopy. 110 (9), 1231-1237 (2010).</li>
<li>Hovden, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Breaking+the+Crowther+limit%3A+combining+depth-sectioning+and+tilt+tomography+for+high-resolution%2C+wide-field+3D+reconstructions%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">Breaking the Crowther limit: combining depth-sectioning and tilt tomography for high-resolution, wide-field 3D reconstructions.</a> Ultramicroscopy. 140, 26-31 (2014).</li>
<li>Dahmen, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Combined+scanning+transmission+electron+microscopy+tilt-+and+focal+series%5BTitle%5D)+AND+%22Microsc+Microanal%22%5BJournal%5D)">Combined scanning transmission electron microscopy tilt- and focal series.</a> Microsc Microanal. 20 (2), 548-560 (2014).</li>
<li>Trepout, S., Messaoudi, C., Perrot, S., Bastin, P., Marco, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Scanning+transmission+electron+microscopy+through-focal+tilt-series+on+biological+specimens%5BTitle%5D)+AND+%22Micron%22%5BJournal%5D)">Scanning transmission electron microscopy through-focal tilt-series on biological specimens.</a> Micron. 77, 9-15 (2015).</li>
<li>Weyland, M., Muller, D. A. <a target="_blank" href="http://muller.research.engineering.cornell.edu/sites/WEELS/summer06/FEI%20nanoSolutions%20Muller.pdf">Tuning the convergence angle for optimum STEM performance.</a> FEI Nanosolutions. 1 (24), (2005).</li>
<li>Schneider, C. A., Rasband, W. S., Eliceiri, K. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((NIH+Image+to+ImageJ%3A+25+years+of+image+analysis%5BTitle%5D)+AND+%22Nat+Methods%22%5BJournal%5D)">NIH Image to ImageJ: 25 years of image analysis.</a> Nat Methods. 9 (7), 671-675 (2012).</li>
<li>Thevenaz, P., Ruttimann, U. E., Unser, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+pyramid+approach+to+subpixel+registration+based+on+intensity%5BTitle%5D)+AND+%22IEEE+Trans+Image+Process%22%5BJournal%5D)">A pyramid approach to subpixel registration based on intensity.</a> IEEE Trans Image Process. 7 (1), 27-41 (1998).</li>
<li>Forster, B., Van De Ville, D., Berent, J., Sage, D., Unser, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Complex+wavelets+for+extended+depth-of-field%3A+a+new+method+for+the+fusion+of+multichannel+microscopy+images%5BTitle%5D)+AND+%22Microsc+Res+Tech%22%5BJournal%5D)">Complex wavelets for extended depth-of-field: a new method for the fusion of multichannel microscopy images.</a> Microsc Res Tech. 65 (1-2), 33-42 (2004).</li>
<li>Messaoudii, C., Boudier, T., Sanchez Sorzano,, O, C., Marco, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((TomoJ%3A+tomography+software+for+three-dimensional+reconstruction+in+transmission+electron+microscopy%5BTitle%5D)+AND+%22BMC+Bioinformatics%22%5BJournal%5D)">TomoJ: tomography software for three-dimensional reconstruction in transmission electron microscopy.</a> BMC Bioinformatics. 8, 288(2007).</li>
<li>Sorzano, C. O., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Marker-free+image+registration+of+electron+tomography+tilt-series%5BTitle%5D)+AND+%22BMC+Bioinformatics%22%5BJournal%5D)">Marker-free image registration of electron tomography tilt-series.</a> BMC Bioinformatics. 10, 124(2009).</li>
<li>Messaoudi, C. , Available from:
 <a target="_blank" href="http://cmib.curie.fr/fr/download/softwares/TomoJ">http://cmib.curie.fr/fr/download/softwares/TomoJ</a> (2016).</li>
<li>Thevenaz, P. , Available from:
 <a target="_blank" href="http://bigwww.epfl.ch/thevenaz/turboreg ">http://bigwww.epfl.ch/thevenaz/turboreg </a> (2016).</li>
<li>Forster, B. , Available from:
 <a target="_blank" href="http://bigwww.epfl.ch/demo/edf/">http://bigwww.epfl.ch/demo/edf/</a> (2016).</li>
<li>Kohl, L., Bastin, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+flagellum+of+trypanosomes%5BTitle%5D)+AND+%22Int+Rev+Cytol%22%5BJournal%5D)">The flagellum of trypanosomes.</a> Int Rev Cytol. 244, 227-285 (2005).</li>
<li>Luft, J. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Improvements+in+epoxy+resin+embedding+methods%5BTitle%5D)+AND+%22J+Biophys+Biochem+Cytol%22%5BJournal%5D)">Improvements in epoxy resin embedding methods.</a> J Biophys Biochem Cytol. 9, 409-414 (1961).</li>
<li>Mielanczyk, L., Matysiak, N., Michalski, M., Buldak, R., Wojnicz, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Closer+to+the+native+state.+Critical+evaluation+of+cryo-techniques+for+Transmission+Electron+Microscopy%3A+preparation+of+biological+samples%5BTitle%5D)+AND+%22Folia+Histochem+Cytobiol%22%5BJournal%5D)">Closer to the native state. Critical evaluation of cryo-techniques for Transmission Electron Microscopy: preparation of biological samples.</a> Folia Histochem Cytobiol. 52 (1), 1-17 (2014).</li>
<li>Hovden, R., Xin, H. L., Muller, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Extended+depth+of+field+for+high-resolution+scanning+transmission+electron+microscopy%5BTitle%5D)+AND+%22Microsc+Microanal%22%5BJournal%5D)">Extended depth of field for high-resolution scanning transmission electron microscopy.</a> Microsc Microanal. 17 (1), 75-80 (2011).</li>
<li>Dahmen, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+Ettention+software+package%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">The Ettention software package.</a> Ultramicroscopy. 161, 110-118 (2016).</li>
<li>Murata, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Whole-cell+imaging+of+the+budding+yeast+Saccharomyces+cerevisiae+by+high-voltage+scanning+transmission+electron+tomography%5BTitle%5D)+AND+%22Ultramicroscopy%22%5BJournal%5D)">Whole-cell imaging of the budding yeast Saccharomyces cerevisiae by high-voltage scanning transmission electron tomography.</a> Ultramicroscopy. 146, 39-45 (2014).</li>
<li>Kizilyaprak, C., Daraspe, J., Humbel, B. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Focused+ion+beam+scanning+electron+microscopy+in+biology%5BTitle%5D)+AND+%22J+Microsc%22%5BJournal%5D)">Focused ion beam scanning electron microscopy in biology.</a> J Microsc. 254 (3), 109-114 (2014).</li>
<li>Kubota, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((New+developments+in+electron+microscopy+for+serial+image+acquisition+of+neuronal+profiles%5BTitle%5D)+AND+%22Microscopy+%28Oxf%29%22%5BJournal%5D)">New developments in electron microscopy for serial image acquisition of neuronal profiles.</a> Microscopy (Oxf). 64 (1), 27-36 (2015).</li>
<li>Levin, B. D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Nanomaterial+datasets+to+advance+tomography+in+scanning+transmission+electron+microscopy%5BTitle%5D)+AND+%22Sci+Data%22%5BJournal%5D)">Nanomaterial datasets to advance tomography in scanning transmission electron microscopy.</a> Sci Data. 3, 160041(2016).</li>
</ol>

We have no conflict of interest to disclose.

In this article, we present a conventional sample preparation protocol along with a step-by-step guide for performing 3D analysis on thick biological samples using STEM through-focal tomography. Resin embedding of biological specimens has been used for decades26, and alternative protocols that are adapted to different kinds of samples can be found throughout the literature27. In contrast, imaging thick specimens in STEM using through-focus methods is a new undertaking, and ...

Since the early 1970s, tomography approaches in transmission electron microscopy (TEM) have been widely used for the structural characterization of biological specimens1,2,3. The appeal of transmission electron tomography was that it could be used to study a wide range of biological structures at the nanometer scale, from the architecture of cells and the ultrastructure of organelles to the structure of macromolecular complexes and proteins. Nevertheless, transmission electron tomography could not be used to study very thick samples (greater than 0.5 &#181;m). Indeed, thick specimens produce too many scattered electrons, generating low signal-to-noise ratio (SNR) images. In addition, tomography involves the collection of images of tilted specimens, with the apparent thickness of the sample increasing with the tilt angle. Even though inelastic scattering can be filtered out using energy filters, the critical amount of electrons needed for high SNR images is barely reached in TEM. Hence, thick biological specimens have only been studied using sectioning4.
Some samples cannot be sliced: some might degrade when they are cut, and others need to be studied in their entirety in order to understand their complexity. An alternative approach is to use TEM in scanning mode5,6,7,8. In scanning transmission electron microscopy (STEM), the optical path of the electrons is different from that in conventional TEM. Electrons passing through the sample without scattering can be collected on the optical axis with a bright-field (BF) detector9, whereas those scattered elastically can be collected at a certain angle from the optical axis with a dark-field (DF) detector. The other advantage of STEM is that the focused electron beam is scanned at the surface of the sample, enabling the pixel-by-pixel collection of the images. Even though the electron beam broadens while passing through the sample10, this particular collection scheme is less sensitive to inelastically scattered electrons than conventional TEM. Furthermore, there is no lens post-specimen in STEM, thereby avoiding the chromatic aberrations that can occur in TEM. The camera length can be adjusted so that the BF detector mainly detects unscattered electrons. Using the DF detector to study thick samples is not recommended because of multiple scattering, which produces inaccurate images. Instead, the BF detector can be used11. While STEM can produce high SNR images, it has a relatively low depth-of-field because of the relatively high beam convergence compared to TEM, decreasing the amount of in-depth information that can be recovered from thick specimens. In the case of aberration-corrected STEM microscopes, where the convergence angle can be as high as 30 mrad, the depth-of-field can be low enough so that the information that is in focus originates from a focal plane of only a few nanometers. Setting up the electron beam in parallel mode enhances the depth-of-field of the electron beam to the detriment of the resolution12. However, this setup is not always possible.
Whenever it is necessary to use a convergent electron beam, one must use techniques that enhance the depth-of-field of the electron beam when studying thick samples. Recent studies have reported the acquisition of multiple images at various focal planes throughout the sample to recover the maximum amount of in-focus information13,14. The two studies describe different ways to handle the information from the different focal planes. Hovden et al. combined in Fourier space the images that were collected at various focal planes, and the final reconstruction was obtained directly from the 3D inverse Fourier transform13. In contrast, Dahmen et al. developed a convergent beam reconstruction engine to reconstruct in real space the 3D volume from the various focal planes14. Our laboratory also developed a method for imaging thick biological specimens. Our strategy was different from the two methods described above in that we merged the information that is in focus in the various focal planes and reconstructed the final 3D volume in real space using a parallel beam projector15. Our aim was to develop a method that can easily be performed in any electron microscopy laboratory. To this end, we aimed to collect the focal images in a limited amount of time, comparable to the time frame of conventional tomography experiments. In addition, our proposed method could be adapted for use with different types of alignment and reconstruction software.
In the context of our publication from 201515, we wanted to visualize and characterize the recovery of the depth-of-field, so we used a large convergence semi-angle of 25 mrad. Here, we present a step-by-step protocol for performing through-focal imaging in STEM according to the method developed in our laboratory in 201515, and we present how the data from 2015 was processed. This method recovers in-focus information from several focal planes throughout a thick (750 nm) biological sample and enables high-quality 3D reconstructions. Where relevant, the differences in this methodology versus the methods used by other groups are also presented.

<table><tbody><tr><td>Phosphate Buffered Saline</td><td>Sigma-Aldrich</td><td>P4417</td><td></td></tr><tr><td>Ethanol</td><td>Sigma-Aldrich</td><td>2860</td><td></td></tr><tr><td>Epoxy resin</td><td>EMS</td><td>14120</td><td></td></tr><tr><td>Paraformaldehyde</td><td>Sigma-Aldrich</td><td>P6148</td><td>Add paraformaldehyde powder to PBS heated at approximately 60 &amp;deg;C.&lt;br/&gt; Increase pH by adding 1 N NaOH until no PFA powder is visible.</td></tr><tr><td>Glutaraldehyde</td><td>Sigma-Aldrich</td><td>G5882&amp;nbsp;</td><td></td></tr><tr><td>Osmium Tetroxyde</td><td>EMS</td><td>19150</td><td></td></tr><tr><td>Uranyl Acetate</td><td>Sigma-Aldrich</td><td>73943</td><td></td></tr><tr><td>Gelatin Capsule</td><td>EMS</td><td>70110</td><td></td></tr><tr><td>Triming and Histo knives</td><td>LFG Distribution</td><td>Diatome diamond knives</td><td></td></tr><tr><td>Electron Microscopy copper grid</td><td>LFG Distribution</td><td>G200-Cu</td><td></td></tr><tr><td>Grid Coating Pen</td><td>LFG Distribution</td><td>70624</td><td></td></tr><tr><td>Specimen Holder</td><td>JEOL</td><td>EM-21311 HTR</td><td></td></tr><tr><td>Electron Microscope</td><td>JEOL</td><td>JEM-2200FS</td><td></td></tr></tbody></table>

preparation and observation of thick biological samples by scanning transmission electron tomography

Preparation and Observation of Thick Biological Samples by Scanning Transmission Electron Tomography

This report describes a protocol for preparing thick biological specimens for further observation using a scanning transmission electron microscope. It also describes an imaging method for studying the 3D structure of thick biological specimens by scanning transmission electron tomography. The sample preparation protocol is based on conventional methods in which the sample is fixed using chemical agents, treated with a heavy atom salt contrasting agent, dehydrated in a series of ethanol baths, and embedded in resin. The specific imaging conditions for observing thick samples by scanning transmission electron microscopy are then described. Sections of the sample are observed using a through-focus method involving the collection of several images at various focal planes. This enables the recovery of in-focus information at various heights throughout the sample. This particular collection pattern is performed at each tilt angle during tomography data collection. A single image is then generated, merging the in-focus information from all the different focal planes. A classic tilt-series dataset is then generated. The advantage of the method is that the tilt-series alignment and reconstruction can be performed using standard tools. The collection of through-focal images allows the reconstruction of a 3D volume that contains all of the structural details of the sample in focus.

In our study, electrons were accelerated to 200 kV in the field emission gun transmission electron microscope. Images were collected in STEM BF mode using a 20-µs dwell time. Regarding the design of the through-focal tilt-series, we found that focus intervals of 150 nm gave satisfactory results for the ultrastructural study of a 750 nm-thick biological sample-even though the depth-of-field of the electron beam was only 3 nm-since we used a very large convergence semi-angle of 25 mrad....

This report describes a sample preparation protocol and specific imaging conditions for performing scanning transmission electron tomography of thick biological specimens.

This report describes a protocol for preparing thick biological specimens for further observation using a scanning transmission electron microscope. It ...

The overall goal of this procedure is to obtain a three-dimensional reconstruction with depth of field recovery of a thick biological specimen using convergent beam scanning transmission electron tomography. This method can answer key questions in the field of structural biology about electron tomography of thick biological specimens. The main advantage of this technique is that images can be acquired in convergent bit mode and the data processing can be performed on most software dedicated to tomography.To begin preparing cell culture sample, centrifuge the sample at 5000 x g for five minutes. Use these centrifugation parameters throughout sample preparation. Discard the supernatant and resuspend the cells in one milliliter of PBS enriched with 4%paraformaldehyde and 2%gluteraldehyde.Incubate the suspension for 30 minutes at room temperature. Centrifuge the mixture, discard the supernatant, and wash the pellet three times with one milliliter portions of PBS. Using the same incubation conditions and washing procedure, incubate the pellet in one milliliter of PBS, enriched with 1%osmium tetroxide, and in one milliliter of PBS enriched with 2%uranyl acetate.Next, cool the sample to four degrees Celsius. Dehydrate the pellet by successive incubations in increasingly concentrated ethanol solutions. Maintaining the sample temperature of four degrees Celsius throughout incubation, centrifugation, and washing.Resuspend the dehydrated pellet in one milliliter of pure ethanol, and incubate overnight at 4 degrees Celsius. Then, allow the sample to warm to room temperature, and centrifuge the sample. Incubate the pellet in increasingly concentrated epoxy resin solutions at room temperature.After the final wash, resuspend the pellet in one milliliter of pure epoxy resin, and incubate overnight at room temperature. Centrifuge the sample, and remove the supernatant, and then resuspend the pellet in 200 microliters of epoxy resin and hardener. Transfer the suspension into the capsule.Incubate the plastic capsule at 60 degrees Celsius for 48 hours to polymerize the resin. Remove the capsule from the incubator and verify resin polymerization. Add a layer of epoxy resin and hardener over the embedded sample and incubate the capsule again under the same conditions.Mount the sample embedded in resin upside down in a specimen holder. Securely fix the sample on the trimming block of an ultramicrotome. Cut the plastic capsule away from the sample in the resin.Shape the exposed resin into a pyramid. Then transfer the capsule and specimen holder to the moving arm of the ultramicrotome. Install a trimming knife and guided by a microscope, refine the pyramid shape.Replace the trimming knife with a histology knife. Under the microscope, adjust the capsule pitch angle so the pyramid is perpendicular to the knife edge. Set the cutting speed and section the sample.After sectioning the sample, transfer the chosen section to a treated copper grid over filter paper. Allow the sample to dry, and then load the sample into the electron microscope. To design the through focal tilt series, first calculate the electron beam depth of field and the maximal apparent thickness of the sample.Based on these values, select a focus interval and determine the number of focal steps needed to image the entire sample at the maximal apparent thickness. Then, at low magnification, locate the region of interest within the sample. Adjust the eucentric height so that the ROI does not appear to move when the sample is rotated.Verify that the ROI remains visible throughout the tilt range. Fill in the through focal tilt series parameters for automated image collection and acquire the images. Import the image series into an image processing program, and align the images collected at the same tilt angle in a pyramidal hierarchy.Find the alignment at each tilt angle by stacking the aligned images. Browse through the stack to ensure that only the focused region moves from image to image and realign the images as needed. Once alignment is verified throughout the sample, merge the in-focus information at the high settings to yield the series with a single image per tilt angle.Perform find alignment of the tilt series based on local minima or fiducial markers. Perform a 3-D reconstruction and inspect the resulting image. If the reconstruction appears blurred or deformed, realign the original image series.A sample of t. brucei was imaged and analyzed using this method. At a zero degree tilt angle, several details of the flagellar pocket are visible.At the higher tilt angle of 70 degrees, only a portion of each image collected in the through focal series is in focus. This position shifts throughout the series. By merging the in-focus sections, a single image with a larger in-focus zone is produced.This effect is even more pronounced when the high frequency areas of the through focal tilt series are highlighted. The high frequency information spans most of the combined image, indicating that the through focal tilt series has been processed well. Once mastered, the image processing part can be done in around three to four hours, depending on the chosen alignment and reconstruction parameters.While attempting this procedure, it's important to remember that the quality of the final reconstruction greatly depends on the quality of the previous alignments tests. After watching this video, you should have a good understanding of how to perform the collection and the image processing of a through focal tilt series.

preparation-observation-thick-biological-samples-scanning

Research

JoVE Journal

Biology

We present a protocol on how to utilize high-throughput cryo-electron tomography to determine high resolution in situ structures of molecular machines. The protocol permits large amounts of data to be processed, avoids common bottlenecks and reduces resource downtime, allowing the user to focus on important biological questions.

Using Tomoauto: A Protocol for High-throughput Automated Cryo-electron Tomography

This study presents reliable and easy procedures for obtaining serial ultrathin sections of a microorganism without expensive equipment in transmission electron microscopy.

A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy

Here, we present detailed processing protocols for imaging delicate tissue samples using scanning electron microscopy (SEM). Three different processing methods, namely, hexamethyl disilazana (HMDS) chemical drying, simple air drying, and critical point drying are described for preparing rigid eggshells, embryos at early developmental stages, and fungal cultures respectively.

Processing Embryo, Eggshell, and Fungal Culture for Scanning Electron Microscopy

We describe the preparation of ribbons of serial sections and their collection on large transfer support for use as Array Tomography samples, along with automated imaging procedures in a scanning electron microscope. The protocol allows screening, retrieval, and targeted imaging of local, rare events, and the acquisition of large data volumes.

Array Tomography Workflow for the Targeted Acquisition of Volume Information using Scanning Electron Microscopy

Using focused ion beam milling to produce vitreous on-grid lamellae from plunge frozen biological samples for cryo-electron tomography.

Preparing Lamellae from Vitreous Biological Samples Using a Dual-Beam Scanning Electron Microscope for Cryo-Electron Tomography

The increasing demand for large-scale data collection in cryogenic electron tomography requires high-throughput image acquisition routines. Described here is a protocol that implements the recent developments of advanced acquisition strategies aimed at maximizing the time-efficiency and throughput of tomographic data collection.

Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition

The present protocol describes high-resolution cryo-electron tomography remote data acquisition using Tomo5 and subsequent data processing and subtomogram averaging using emClarity. Apoferritin is used as an example to illustrate detailed step-by-step processes to achieve a cryo-ET structure at 2.86 Å resolution.

Cryo-Electron Tomography Remote Data Collection and Subtomogram Averaging

Cryo-STEM tomography provides a means to visualize organelles of intact cells without embedding, sectioning, or other invasive preparations. The 3D resolution obtained is currently in the range of a few nanometers, with a field of view of several micrometers and an accessible thickness in the order of 1 µm.

Visualization of Organelles In Situ by Cryo-STEM Tomography

This video protocol illustrates how to perform scanning transmission electron microscopy tomography of virological specimens. For optimal outcomes, samples are prepared by high-pressure freezing and subsequent freeze substitution.

Scanning Transmission Electron Microscopy Tomography in Virology: 3D Imaging of High-pressure Frozen, Freeze-substituted Samples

We present a protocol of how to collect and process electron cryo-tomograms of whole mitochondria. The technique provides detailed insights into the structure, function, and organization of large membrane protein complexes in native biological membranes.

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography

Learn scanning transmission electron tomography for structural biology using convergent beam imaging of thick biological specimens. This method enables three-dimensional reconstruction with depth of field recovery for detailed analysis.

Preparation and Observation of Thick Biological Samples by Scanning Transmission Electron Tomography

Explore More Videos