Abstract

Sample preparation is critical to biological electron microscopy (EM), and there have been continuous efforts on optimizing the procedures to best preserve structures of interest in the sample. However, a quantitative characterization of the morphological changes associated with each step in EM sample preparation is currently lacking. Using correlative EM and superresolution microscopy (SRM), we have examined the effects of different drying methods as well as osmium tetroxide (OsO4) post-fixation on cell morphology during scanning electron microscopy (SEM) sample preparation. Here, SRM images of the sample acquired under hydrated conditions were used as a baseline for evaluating morphological changes as the sample went through SEM sample processing. We found that both chemical drying and critical point drying lead to a mild cellular boundary retraction of ~60 nm. Post-fixation by OsO4 causes at least 40 nm additional boundary retraction. We also found that coating coverslips with adhesion molecules such as fibronectin prior to cell plating helps reduce cell distortion from OsO4 post-fixation. These quantitative measurements offer useful information for identifying causes of cell distortions in SEM sample preparation and improving current procedures.

Highlights

  • Scanning electron microscopy (SEM) is extensively used to study structural details on the surface of biological samples

  • We found that the dehydration and drying steps caused a mild boundary retraction at an average of 60 nm to cells cultured on glass, and the effect was similar between Critical point drying (CPD) and chemical drying using HMDS

  • For workflows that perform superresolution microscopy (SRM) before EM, it is important to ensure that the cell morphology is well preserved when the sample goes through the preparation steps

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Summary

Introduction

Scanning electron microscopy (SEM) is extensively used to study structural details on the surface of biological samples. The conventional sample preparation process for SEM includes fixation, dehydration, drying, and optionally, conductive coating. Fixation is typically performed in aldehyde buffer; in certain cases, this is followed by a post-fixation step in osmium tetroxide (OsO4) or uranyl acetate (UA). The sample is first dehydrated with organic solvents to replace water and dried to remove the organic solvents. Each of these steps, i.e., fixation, dehydration, and drying, can introduce artifacts into delicate biological samples such.

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