Literature DB >> 27320699

Long shelf-life streptavidin support-films suitable for electron microscopy of biological macromolecules.

Bong-Gyoon Han1, Zoe Watson2, Hannah Kang1, Arto Pulk3, Kenneth H Downing1, Jamie Cate4, Robert M Glaeser5.   

Abstract

We describe a rapid and convenient method of growing streptavidin (SA) monolayer crystals directly on holey-carbon EM grids. As expected, these SA monolayer crystals retain their biotin-binding function and crystalline order through a cycle of embedding in trehalose and, later, its removal. This fact allows one to prepare, and store for later use, EM grids on which SA monolayer crystals serve as an affinity substrate for preparing specimens of biological macromolecules. In addition, we report that coating the lipid-tail side of trehalose-embedded monolayer crystals with evaporated carbon appears to improve the consistency with which well-ordered, single crystals are observed to span over entire, 2μm holes of the support films. Randomly biotinylated 70S ribosomes are used as a test specimen to show that these support films can be used to obtain a high-resolution cryo-EM structure.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Affinity grid; Electron microscopy; Streptavidin

Mesh:

Substances:

Year:  2016        PMID: 27320699      PMCID: PMC4943657          DOI: 10.1016/j.jsb.2016.06.009

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


  22 in total

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Review 3.  Retrospective on the early development of cryoelectron microscopy of macromolecules and a prospective on opportunities for the future.

Authors:  Kenneth A Taylor; Robert M Glaeser
Journal:  J Struct Biol       Date:  2008-06-19       Impact factor: 2.867

4.  Liposomes on a streptavidin crystal: a system to study membrane proteins by cryo-EM.

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Journal:  Methods Enzymol       Date:  2010       Impact factor: 1.600

5.  Structure of the E. coli ribosome-EF-Tu complex at <3 Å resolution by Cs-corrected cryo-EM.

Authors:  Niels Fischer; Piotr Neumann; Andrey L Konevega; Lars V Bock; Ralf Ficner; Marina V Rodnina; Holger Stark
Journal:  Nature       Date:  2015-02-23       Impact factor: 49.962

6.  Streptavidin crystals as nanostructured supports and image-calibration references for cryo-EM data collection.

Authors:  Liguo Wang; Puey Ounjai; Fred J Sigworth
Journal:  J Struct Biol       Date:  2008-08-05       Impact factor: 2.867

7.  Measuring the optimal exposure for single particle cryo-EM using a 2.6 Å reconstruction of rotavirus VP6.

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8.  Ribosome structures to near-atomic resolution from thirty thousand cryo-EM particles.

Authors:  Xiao-Chen Bai; Israel S Fernandez; Greg McMullan; Sjors H W Scheres
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  18 in total

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Review 4.  Biological Applications at the Cutting Edge of Cryo-Electron Microscopy.

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5.  Monolayer-crystal streptavidin support films provide an internal standard of cryo-EM image quality.

Authors:  Bong-Gyoon Han; Zoe Watson; Jamie H D Cate; Robert M Glaeser
Journal:  J Struct Biol       Date:  2017-03-01       Impact factor: 2.867

6.  From Tube to Structure: SPA Cryo-EM Workflow Using Apoferritin as an Example.

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Journal:  Methods Mol Biol       Date:  2021

Review 7.  Cryo-EM: beyond the microscope.

Authors:  Lesley A Earl; Veronica Falconieri; Jacqueline Ls Milne; Sriram Subramaniam
Journal:  Curr Opin Struct Biol       Date:  2017-06-21       Impact factor: 6.809

8.  Cryo-EM studies of NAIP-NLRC4 inflammasomes.

Authors:  Nicole Haloupek; Patricia Grob; Jeannette Tenthorey; Russell E Vance; Eva Nogales
Journal:  Methods Enzymol       Date:  2019-05-24       Impact factor: 1.600

9.  A simple and robust procedure for preparing graphene-oxide cryo-EM grids.

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Journal:  J Struct Biol       Date:  2018-07-11       Impact factor: 2.867

10.  JARID2 and AEBP2 regulate PRC2 in the presence of H2AK119ub1 and other histone modifications.

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Journal:  Science       Date:  2021-01-22       Impact factor: 47.728

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