Abstract

Phase contrast transmission electron microscopy (TEM) based on thin-film phase plates has been developed and applied to biological systems. Currently, development is focused on two techniques that employ two different types of phase plates. The first technique uses a Zernike phase plate, which is made of a uniform amorphous carbon film that completely covers the aperture of an objective lens and can retard the phase of electron waves by π/2, except at the centre where a tiny hole is drilled. The other technique uses a Hilbert phase plate, which is made of an amorphous carbon film that is twice as thick as the Zernike phase plate, covers only half of the aperture and retards the electron wave phase by π. By combining the power of efficient phase contrast detection with the accurate preservation achieved by a cryotechnique such as vitrification, macromolecular complexes and supermolecular structures inside intact bacterial or eukaryotic cells may be visualized without staining. Phase contrast cryo-TEM has the potential to bridge the gap between cellular and molecular biology in terms of high-resolution visualization. Examples using proteins, viruses, cyanobacteria and somatic cells are provided.

Highlights

  • Biological transmission electron microscopy (TEM) has enabled visualization of many heretofore ‘invisible’ substances, including those that are soft, fragile or hydrous

  • By positioning the beam very close to the phase plate edge, the phase contrast transfer can be extended to much lower frequencies, which results in higher contrast images than those obtained by CTEM and Zernike phase contrast (ZPC)-TEM

  • ZPC-TEM promises to be the third method able to significantly increase the visibility of viruses in their intact form

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Summary

INTRODUCTION

Biological transmission electron microscopy (TEM) has enabled visualization of many heretofore ‘invisible’ substances, including those that are soft, fragile or hydrous. Examples of biological sample transformations (and the respective techniques involved) include the conversion of soft substances to hard (chemical fixation), hydrous to non-hydrous (dehydration), fragile to robust (resin embedding) and the invisible to the visible (staining). These techniques have enriched the realm of microbiology and biological TEM, but are usually highly time-consuming, and the return is currently considered small compared with other methods. A fundamental problem with the application of this method to biological specimens is the resolution deterioration by defocusing The solution to this problem in light microscopy suggests a similar approach here: a phase contrast method that uses phase plates.

METHODS
20 Å number of particles
Findings
DISCUSSIONS AND CONCLUSIONS
Full Text
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