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J Am Chem Soc. 2012 May 30;134(21):8823-30. doi: 10.1021/ja2110703. Epub 2012 Mar 13.

RNA encapsidation by SV40-derived nanoparticles follows a rapid two-state mechanism.

Author information

1
Department of Hematology, Hebrew University-Hadassah Medical School, Jerusalem, Israel 91120.

Abstract

Remarkably, uniform virus-like particles self-assemble in a process that appears to follow a rapid kinetic mechanism. The mechanisms by which spherical viruses assemble from hundreds of capsid proteins around nucleic acid, however, are yet unresolved. Using time-resolved small-angle X-ray scattering (TR-SAXS), we have been able to directly visualize SV40 VP1 pentamers encapsidating short RNA molecules (500mers). This assembly process yields T = 1 icosahedral particles comprised of 12 pentamers and one RNA molecule. The reaction is nearly one-third complete within 35 ms, following a two-state kinetic process with no detectable intermediates. Theoretical analysis of kinetics, using a master equation, shows that the assembly process nucleates at the RNA and continues by a cascade of elongation reactions in which one VP1 pentamer is added at a time, with a rate of approximately 10(9) M(-1) s(-1). The reaction is highly robust and faster than the predicted diffusion limit. The emerging molecular mechanism, which appears to be general to viruses that assemble around nucleic acids, implicates long-ranged electrostatic interactions. The model proposes that the growing nucleo-protein complex acts as an electrostatic antenna that attracts other capsid subunits for the encapsidation process.

PMID:
22329660
PMCID:
PMC3365646
DOI:
10.1021/ja2110703
[Indexed for MEDLINE]
Free PMC Article

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