Breadcrumb
- Home
- Publications
- Proceedings
- 2009 Annual Meeting
- Engineering Sciences and Fundamentals
- Thermophysical Properties of Biological Systems - II
- (638b) Generalized Structural Polymorphism in Virus Capsid Self-Assembly
We observed, in addition to icosahedral capsids, a variety of nonicosahedral yet highly ordered and enclosed capsules. Such structural polymorphism was demonstrated to be an inherent property of the coat proteins, independent of the capsid complexity and the elementary kinetic mechanisms. Moreover, there exist two distinctive classes of polymorphic structures: aberrant capsules that are larger than their respective icosahedral capsids when T = 1-7; and capsules that are smaller than their respective icosahedral capsids when T = 7-19. Different kinetic mechanisms responsible for self-assembly of those classes of aberrant structures were deciphered, providing insights into the control of the self-assembly of icosahedral capsids.
References:
1. H.D. Nguyen, V.S. Reddy and C.L. Brooks III, ?Deciphering the kinetic mechanism of spontaneous self-assembly of icosahedral capsids,? Nano Letters, 7(2) 338-44 (2007)
2. H.D. Nguyen, V.S. Reddy and C.L. Brooks III, ?Invariant polymorphism in virus capsid assembly,? J. Am. Chem. Soc., 131(7): 2606-14 (2009)
3. H.D. Nguyen and C.L. Brooks III, ?Generalized structural polymorphism of self-assembled viral capsids,? Nano Letters, 8(12), 4574-81 (2008)