scholarly journals Dual-axis Volta phase plate cryo-electron tomography of Ebola virus-like particles reveals actin-VP40 interactions

2021 ◽  
Author(s):  
Sophie L. Winter ◽  
Petr Chlanda

AbstractCryo-electron tomography (cryo-ET) is a pivotal imaging technique for studying the structure of pleomorphic enveloped viruses and their interactions with the host at native conditions. Owing to the limited tilting range of samples with a slab geometry, electron tomograms suffer from so-called missing wedge information in Fourier space. In dual-axis cryo-ET, two tomograms reconstructed from orthogonally oriented tilt series are combined into a tomogram with improved resolution as the missing wedge information is reduced to a pyramid. Volta phase plate (VPP) allows to perform in-focus cryo-ET with high contrast transfer at low-resolution frequencies and thus its application may improve the quality of dual-axis tomograms. Here, we compare dual-axis cryo-ET with and without VPP on Ebola virus-like particles to visualize and segment viral and host cell proteins within the membrane-enveloped filamentous particles. Dual-axis VPP cryo-ET reduces the missing wedge information and ray artifacts arising from the weighted back-projection during tomogram reconstruction, thereby minimizing ambiguity in the analysis of crowded environments and facilitating 3D segmentation. We show that dual-axis VPP tomograms provide a comprehensive description of macromolecular organizations such as nucleocapsid assembly states, the distribution of glycoproteins on the viral envelope and asymmetric arrangements of the VP40 layer in non-filamentous regions of virus-like particles. Our data reveal actin filaments within virus-like particles in close proximity to the viral VP40 scaffold, suggesting a direct interaction between VP40 and actin filaments. Dual-axis VPP cryo-ET provides more complete 3D information at high contrast and allows for better interpretation of macromolecule interactions and pleomorphic organizations.HighlightsVolta phase plate dual-axis cryo-electron tomography provides high contrast tomography data with reduced back-projection ray artifacts and missing wedge information in Fourier spaceVolta phase plate dual-axis cryo-electron tomography facilitates interpretation of protein-membrane interactionsVolta phase plate dual-axis cryo-electron tomography reduces ambiguity in manual 3D rendering and markedly improves 3D isosurface modelingEbola virus-like particles contain actin filaments in close proximity to the VP40 layer

2016 ◽  
Vol 22 (S3) ◽  
pp. 74-75
Author(s):  
Z. Hong Zhou ◽  
Wong H. Hui ◽  
Jiayan Zhang ◽  
Ivo Atanasov ◽  
Cristina C. Celma ◽  
...  

2014 ◽  
Vol 20 (S3) ◽  
pp. 232-233
Author(s):  
Maryam Khoshouei ◽  
Radostin Danev ◽  
Günther Gerisch ◽  
Maria Ecke ◽  
Juergen Plitzko ◽  
...  

2018 ◽  
Vol 14 (12) ◽  
pp. e1007452 ◽  
Author(s):  
Zhu Si ◽  
Jiayan Zhang ◽  
Sakar Shivakoti ◽  
Ivo Atanasov ◽  
Chang-Lu Tao ◽  
...  

2016 ◽  
Vol 110 (3) ◽  
pp. 250a-251a
Author(s):  
Petr Chlanda ◽  
Elena Mekhedov ◽  
Hang Waters ◽  
Cindi L. Schwartz ◽  
Elizabeth R. Fischer ◽  
...  

2010 ◽  
Vol 16 (S2) ◽  
pp. 546-547
Author(s):  
M Marko ◽  
C Hsieh ◽  
A Leith ◽  
C Mannella

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.


2014 ◽  
Vol 20 (S3) ◽  
pp. 234-235 ◽  
Author(s):  
Haixin Sui ◽  
Gregory Kishchenko ◽  
Radostin Danev ◽  
Jie He ◽  
Rebecca Fisher ◽  
...  

Author(s):  
Petra Kiesel ◽  
Gonzalo Alvarez Viar ◽  
Nikolai Tsoy ◽  
Riccardo Maraspini ◽  
Alf Honigmann ◽  
...  

AbstractPrimary cilia are microtubule-based organelles involved in key signaling and sensing processes in eukaryotic cells. Unlike motile cilia, which have been thoroughly studied, the structure and the composition of primary cilia remain largely unexplored despite their fundamental role in development and homeostasis. They have for long been falsely regarded as simplified versions of motile cilia because they lack distinctive elements such as dynein arms, radial spokes, and central pair complex. However, revealing the detailed molecular composition and 3D structure of primary cilia is necessary in order to understand the mechanisms that govern their functions. Such structural investigations are so far being precluded by the challenging preparation of primary cilia for cryo-electron microscopy. Here, we developed an enabling method for investigating the structure of primary cilia at molecular resolution by cryo-electron tomography. We show that the well-known “9+0” arrangement of microtubule doublets is present only at the base of the primary cilium. A few microns away from the base the ciliary architecture changes into an unstructured bundle of EB1-decorated microtubule singlets and some actin filaments. Our results suggest the existence of a previously unobserved crosstalk between actin filaments and microtubules in the primary cilium. Our work provides unprecedented insights into the molecular structure of primary cilia and a general framework for uncovering their molecular composition and function in health and disease. This opens up new possibilities to study aspects of this important organelle that have so far been out of reach.


2017 ◽  
Vol 23 (S1) ◽  
pp. 1234-1235
Author(s):  
Yoshiyuki Fukuda ◽  
Florian Beck ◽  
Istvan Nagy ◽  
Radostin Danev ◽  
Wolfgang Baumeister

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