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PMID: 19804738 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Elucidating the mechanism behind irreversible deformation of viral capsids.

Biophysical journal ·Vol. 97 ·No. 7 ·2009-10-07 ·Pages 2061-9

Arkhipov A, Roos WH, Wuite GJ, Schulten K

Abstract

Atomic force microscopy has recently provided highly precise measurements of mechanical properties of various viruses. However, molecular details underlying viral mechanics remain unresolved. Here we report atomic force microscopy nanoindentation experiments on T=4 hepatitis B virus (HBV) capsids combined with coarse-grained molecular dynamics simulations, which permit interpretation of experimental results at the molecular level. The force response of the indented capsid recorded in simulations agrees with experimental observations. In both experiment and simulation, irreversible capsid deformation is observed for deep indentations. Simulations show the irreversibility to be due to local bending and shifting of capsid proteins, rather than their global rearrangement. These results emphasize the viability of large capsid deformations without significant changes of the mutual positions of HBV capsid proteins, in contrast to the stiffer capsids of other viruses, which exhibit more extensive contacts between their capsid proteins than seen in the case of HBV.

MeSH Terms
Capsid/chemistry,metabolism Hepatitis B virus Materials Testing Microscopy, Atomic Force Molecular Conformation Molecular Dynamics Simulation Nanotechnology
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Arkhipov Anton
Department of Physics and Beckman Institute, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Roos Wouter H
Wuite Gijs J L
Schulten Klaus
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
1542-0086
Published
2009-10-07
Pages
2061-9
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC2756377
Subset
IM
Grants
NCRR NIH HHS · P41 RR005969 · United States
NCRR NIH HHS · P41-RR005969 · United States
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