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PMID: 17157314 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Distinguishing reversible from irreversible virus capsid assembly.

Journal of molecular biology ·Vol. 366 ·No. 1 ·2007-02-09 ·Pages 14-8

Zlotnick A

Abstract

Capsids of spherical viruses may be constructed from hundreds or thousands of copies of the major capsid protein(s). These assembly reactions are poorly understood. Here we consider the predicted behavior for assembly where the component reactions have weak association energy and are reversible and compare them to essentially irreversible reactions. The comparisons are based on mass action calculations and the behavior predicted from kinetic simulations where assembly is described as a cascade of low order reactions. Reversible reactions are characterized by a pseudo-critical concentration, whereas irreversible reactions consume all free subunits. Irreversible reactions are more susceptible to kinetic traps comprised of numerous small intermediates. In the case where only the ultimate step is irreversible, very low concentrations of intermediates slow the completion of the reaction so that overall it closely matches the predictions for the reversible reactions that make up the majority of the cascade. Data in the literature strongly support the hypothesis that most viruses are held together by many weak interactions.

MeSH Terms
Capsid/chemistry Computer Simulation Forecasting Kinetics Models, Theoretical Thermodynamics Virus Assembly
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Zlotnick Adam
Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. adam-zlotnick@ouhsc.edu
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Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
2007-02-09
Epub
2006-00-11
Pages
14-8
Language
English
Region
England
NLM ID
2985088R
PMCID
PMC1941720
Subset
IM
Grants
NIAID NIH HHS · R01 AI067417 · United States
NIAID NIH HHS · R01 AI 067417 · United States
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