Literature DB >> 8475604

Prospects for using an IVEM with a FEG for imaging macromolecules towards atomic resolution.

Z H Zhou1, W Chiu.   

Abstract

Specimen preparation and imaging techniques for biological macromolecules have been improved to the point where attention to the electron-optical imaging conditions becomes a significant factor for achieving high resolution. A field emission gun (FEG) can provide an illumination source with a better spatial and temporal coherence suitable for imaging near atomic resolution. Our computational analysis of carbon film images taken between Scherzer focus and 1.1 microns underfocus (20x Scherzer focus) with the Hitachi 200 kV microscope with a cold field emission gun shows detectable contrast beyond 3.5 A resolution. In biological imaging, a large defocus is often used to optimize the low-resolution contrast in order to facilitate the subsequent steps in computer reconstruction. An intermediate-voltage electron microscope (IVEM) would optimize the contrast at high resolution by reducing the temporal coherent effects. In theory, the IVEM would give a greater depth of field so that large macromolecular assemblies such as viruses and cellular structures can be interpreted and reconstructed reliably using the projection approximation. These experimental and theoretical considerations provide a rationale for designing a future IVEM with a FEG suitable for biological macromolecule imaging close to atomic resolution.

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Year:  1993        PMID: 8475604     DOI: 10.1016/0304-3991(93)90246-t

Source DB:  PubMed          Journal:  Ultramicroscopy        ISSN: 0304-3991            Impact factor:   2.689


  11 in total

Review 1.  Adding the third dimension to virus life cycles: three-dimensional reconstruction of icosahedral viruses from cryo-electron micrographs.

Authors:  T S Baker; N H Olson; S D Fuller
Journal:  Microbiol Mol Biol Rev       Date:  1999-12       Impact factor: 11.056

2.  Direct electron detection yields cryo-EM reconstructions at resolutions beyond 3/4 Nyquist frequency.

Authors:  Benjamin E Bammes; Ryan H Rochat; Joanita Jakana; Dong-Hua Chen; Wah Chiu
Journal:  J Struct Biol       Date:  2012-01-21       Impact factor: 2.867

3.  Achievable resolution from images of biological specimens acquired from a 4k x 4k CCD camera in a 300-kV electron cryomicroscope.

Authors:  Dong-Hua Chen; Joanita Jakana; Xiangan Liu; Michael F Schmid; Wah Chiu
Journal:  J Struct Biol       Date:  2008-04-14       Impact factor: 2.867

4.  Single-particle selection and alignment with heavy atom cluster-antibody conjugates.

Authors:  G J Jensen; R D Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

5.  Refinement of herpesvirus B-capsid structure on parallel supercomputers.

Authors:  Z H Zhou; W Chiu; K Haskell; H Spears; J Jakana; F J Rixon; L R Scott
Journal:  Biophys J       Date:  1998-01       Impact factor: 4.033

6.  Practical performance evaluation of a 10k × 10k CCD for electron cryo-microscopy.

Authors:  Benjamin E Bammes; Ryan H Rochat; Joanita Jakana; Wah Chiu
Journal:  J Struct Biol       Date:  2011-05-17       Impact factor: 2.867

Review 7.  Current strategies for protein production and purification enabling membrane protein structural biology.

Authors:  Aditya Pandey; Kyungsoo Shin; Robin E Patterson; Xiang-Qin Liu; Jan K Rainey
Journal:  Biochem Cell Biol       Date:  2016-01-20       Impact factor: 3.626

Review 8.  Limiting factors in atomic resolution cryo electron microscopy: no simple tricks.

Authors:  Xing Zhang; Z Hong Zhou
Journal:  J Struct Biol       Date:  2011-05-24       Impact factor: 2.867

Review 9.  Single-Particle Cryo-EM at Crystallographic Resolution.

Authors:  Yifan Cheng
Journal:  Cell       Date:  2015-04-23       Impact factor: 41.582

Review 10.  Towards atomic resolution structural determination by single-particle cryo-electron microscopy.

Authors:  Z Hong Zhou
Journal:  Curr Opin Struct Biol       Date:  2008-04-09       Impact factor: 6.809

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