Literature DB >> 16987672

Electron energy filtering significantly improves amplitude contrast of frozen-hydrated protein at 300kV.

Koji Yonekura1, Michael B Braunfeld, Saori Maki-Yonekura, David A Agard.   

Abstract

The amplitude contrast of frozen-hydrated biological samples was measured using the bacterial flagellar filament embedded in vitreous ice at an accelerating voltage of 300kV. From the mean radial amplitude spectra of overfocused images, amplitude contrast was estimated to be 6.9+/-1.9% and 2.7+/-1.0% of the whole contrast at the low spatial frequency range with and without energy filtering, respectively, and that of the carbon film to be 9.5+/-2.0% and 5.8+/-1.8%. Energy filtering effectively doubled the signal-to-noise ratio in the images of frozen-hydrated filaments, and substantially improved intensity data statistics of layer lines up to at least approximately 25A resolution in their Fourier transforms. It also markedly improved inter-particle fitting phase residuals of averaged data at resolutions up to approximately 15A. Using the energy filtered data recorded on a new high-performance, lens-coupled CCD camera the three-dimensional map of the flagellar filament was calculated at 8A by applying the amplitude contrast of 6.9%. The map and its mean radial density distribution validated the obtained value of the amplitude contrast.

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Year:  2006        PMID: 16987672     DOI: 10.1016/j.jsb.2006.07.016

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  21 in total

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2.  Structures of capsid and capsid-associated tegument complex inside the Epstein-Barr virus.

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Journal:  Nat Microbiol       Date:  2020-07-27       Impact factor: 17.745

3.  On the feasibility of visualizing ultrasmall gold labels in biological specimens by STEM tomography.

Authors:  A A Sousa; M A Aronova; Y C Kim; L M Dorward; G Zhang; R D Leapman
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4.  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

Review 5.  Reaching the information limit in cryo-EM of biological macromolecules: experimental aspects.

Authors:  Robert M Glaeser; Richard J Hall
Journal:  Biophys J       Date:  2011-05-18       Impact factor: 4.033

Review 6.  Determination of the ribosome structure to a resolution of 2.5 Å by single-particle cryo-EM.

Authors:  Zheng Liu; Cristina Gutierrez-Vargas; Jia Wei; Robert A Grassucci; Ming Sun; Noel Espina; Susan Madison-Antenucci; Liang Tong; Joachim Frank
Journal:  Protein Sci       Date:  2016-10-26       Impact factor: 6.725

7.  Benefits and Limitations of Low-kV Macromolecular Imaging of Frozen-Hydrated Biological Samples.

Authors:  Endre Majorovits; Isabel Angert; Ute Kaiser; Rasmus R Schröder
Journal:  Biophys J       Date:  2016-02-23       Impact factor: 4.033

8.  Routine determination of ice thickness for cryo-EM grids.

Authors:  William J Rice; Anchi Cheng; Alex J Noble; Edward T Eng; Laura Y Kim; Bridget Carragher; Clinton S Potter
Journal:  J Struct Biol       Date:  2018-07-04       Impact factor: 2.867

9.  High-resolution electron microscopy of helical specimens: a fresh look at tobacco mosaic virus.

Authors:  Carsten Sachse; James Z Chen; Pierre-Damien Coureux; M Elizabeth Stroupe; Marcus Fändrich; Nikolaus Grigorieff
Journal:  J Mol Biol       Date:  2007-06-04       Impact factor: 5.469

10.  A bipolar spindle of antiparallel ParM filaments drives bacterial plasmid segregation.

Authors:  P Gayathri; T Fujii; J Møller-Jensen; F van den Ent; K Namba; J Löwe
Journal:  Science       Date:  2012-10-25       Impact factor: 47.728

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