| Literature DB >> 16781757 |
Myriam Troesch1, Isabelle Meunier, Pascal Lapierre, Normand Lapointe, Fernando Alvarez, Marc Boucher, Hugo Soudeyns.
Abstract
A large share of hepatitis C virus amino acid sequence variation is concentrated within two hypervariable regions located at the N-terminus of the E2 envelope glycoprotein (HVR1 and HVR2). Interhost and intrahost comparison of 391 E2 sequences derived from 17 subjects infected with HCV using amino acid entropy revealed clustering of amino acid variability at a third site (residues 431-466), which was termed HVR3. Genetic distance analysis supported the division of HVR3 into three subdomains (HVR3a, HVR3b, and HVR3c). Study of synonymous and nonsynonymous nucleic acid substitutions confirmed that HVR3a was subjected to strong intrahost-selective pressure. Physicochemical and antigenicity predictions, conservation of key residues, and molecular modeling were concordant with one another and further validated the proposed organization of HVR3. Taken together, these results are suggestive of a role for HVR3 in cell surface receptor binding and viral entry akin to that proposed for HVR1 and HVR2.Entities:
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Year: 2006 PMID： 16781757 DOI： 10.1016/j.virol.2006.05.015
Source DB: PubMed Journal: Virology ISSN： 0042-6822 Impact factor: 3.616