| Literature DB >> 25172800 |
Matteo Castelli1, Nicola Clementi1, Giuseppe A Sautto1, Jennifer Pfaff2, Kristen M Kahle2, Trevor Barnes2, Benjamin J Doranz2, Matteo Dal Peraro3, Massimo Clementi1, Roberto Burioni1, Nicasio Mancini4.
Abstract
The lack of structural information on hepatitis C virus (HCV) surface proteins has so far hampered the development of effective vaccines. Recently, two crystallographic structures have described the core portion (E2c) of E2 surface glycoprotein, the primary mediator of HCV entry. Despite the importance of these studies, the E2 overall structure is still unknown and, most importantly, several biochemical and functional studies are in disagreement with E2c structures. Here, the main literature will be discussed and an alternative disulfide bridge pattern will be proposed, based on unpublished human monoclonal antibody reactivity. A modeling strategy aiming at recapitulating the available structural and functional studies of E2 will also be proposed.Entities:
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Year: 2014 PMID: 25172800 PMCID: PMC4706463 DOI: 10.1016/j.drudis.2014.08.011
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851