Single particle and molecular assembly analysis of polyribosomes by single- and double-tilt cryo electron tomography

2013 ◽  
Vol 126 ◽  
pp. 33-39 ◽  
Author(s):  
Alexander G. Myasnikov ◽  
Zhanna A. Afonina ◽  
Bruno P. Klaholz
2014 ◽  
Vol 20 (S3) ◽  
pp. 232-233
Author(s):  
Maryam Khoshouei ◽  
Radostin Danev ◽  
Günther Gerisch ◽  
Maria Ecke ◽  
Juergen Plitzko ◽  
...  

2016 ◽  
Vol 194 (3) ◽  
pp. 383-394 ◽  
Author(s):  
Jesús G. Galaz-Montoya ◽  
Corey W. Hecksel ◽  
Philip R. Baldwin ◽  
Eryu Wang ◽  
Scott C. Weaver ◽  
...  

2017 ◽  
Author(s):  
Alex J. Noble ◽  
Venkata P. Dandey ◽  
Hui Wei ◽  
Julia Brasch ◽  
Jillian Chase ◽  
...  

AbstractSingle particle cryo-electron microscopy (cryoEM) is often performed under the assumption that particles are freely floating away from the air-water interfaces and in thin, vitreous ice. In this study, we performed fiducial-less tomography on over 50 different cryoEM grid/sample preparations to determine the particle distribution within the ice and the overall geometry of the ice in grid holes. Surprisingly, by studying particles in holes in 3D from over 1,000 tomograms, we have determined that the vast majority of particles (approximately 90%) are adsorbed to an air-water interface. The implications of this observation are wide-ranging, with potential ramifications regarding protein denaturation, conformational change, and preferred orientation. We also show that fiducial-less cryo-electron tomography on single particle grids may be used to determine ice thickness, optimal single particle collection areas and strategies, particle heterogeneity, and de novo models for template picking and single particle alignment.


2012 ◽  
Vol 1 (2) ◽  
pp. e201207002 ◽  
Author(s):  
Mikhail Kudryashev ◽  
Daniel Castaño-Díez ◽  
Henning Stahlberg

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Geoff Sutton ◽  
Dapeng Sun ◽  
Xiaofeng Fu ◽  
Abhay Kotecha ◽  
Corey W. Hecksel ◽  
...  

Abstract Traditionally, molecular assembly pathways for viruses are inferred from high resolution structures of purified stable intermediates, low resolution images of cell sections and genetic approaches. Here, we directly visualise an unsuspected ‘single shelled’ intermediate for a mammalian orthoreovirus in cryo-preserved infected cells, by cryo-electron tomography of cellular lamellae. Particle classification and averaging yields structures to 5.6 Å resolution, sufficient to identify secondary structural elements and produce an atomic model of the intermediate, comprising 120 copies each of protein λ1 and σ2. This λ1 shell is ‘collapsed’ compared to the mature virions, with molecules pushed inwards at the icosahedral fivefolds by ~100 Å, reminiscent of the first assembly intermediate of certain prokaryotic dsRNA viruses. This supports the supposition that these viruses share a common ancestor, and suggests mechanisms for the assembly of viruses of the Reoviridae. Such methodology holds promise for dissecting the replication cycle of many viruses.


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