| Literature DB >> 27120684 |
Didier Law-Hine1, Anil K Sahoo2, Virginie Bailleux1, Mehdi Zeghal1, Sylvain Prevost3, Prabal K Maiti2, Stéphane Bressanelli4, Doru Constantin1, Guillaume Tresset1.
Abstract
Viral capsids derived from an icosahedral plant virus widely used in physical and nanotechnological investigations were fully dissociated into dimers by a rapid change of pH. The process was probed in vitro at high spatiotemporal resolution by time-resolved small-angle X-ray scattering using a high brilliance synchrotron source. A powerful custom-made global fitting algorithm allowed us to reconstruct the most likely pathway parametrized by a set of stoichiometric coefficients and to determine the shape of two successive intermediates by ab initio calculations. None of these two unexpected intermediates was previously identified in self-assembly experiments, which suggests that the disassembly pathway is not a mirror image of the assembly pathway. These findings shed new light on the mechanisms and the reversibility of the assembly/disassembly of natural and synthetic virus-based systems. They also demonstrate that both the structure and dynamics of an increasing number of intermediate species become accessible to experiments.Keywords: Virus; disassembly; kinetic pathway; modeling; time-resolved small-angle X-ray scattering
Mesh:
Year: 2015 PMID: 27120684 DOI: 10.1021/acs.jpclett.5b01478
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475