HCV E2 core structures and mAbs: something is still missing

被引:24
作者
Castelli, Matteo [1 ]
Clementi, Nicola [1 ]
Sautto, Giuseppe A. [1 ]
Pfaff, Jennifer [2 ]
Kahle, Kristen M. [2 ]
Barnes, Trevor [2 ]
Doranz, Benjamin J. [2 ]
Dal Peraro, Matteo [3 ,4 ]
Clementi, Massimo [1 ]
Burioni, Roberto [1 ]
Mancini, Nicasio [1 ]
机构
[1] Univ Vita Salute San Raffaele, Lab Microbiol & Virol, Milan, Italy
[2] Integral Mol, Philadelphia, PA USA
[3] Ecole Polytech Fed Lausanne, Sch Life Sci, Lab Biomol Modeling, Inst Bioengn, Lausanne, Switzerland
[4] Swiss Inst Bioinformat, Lausanne, Switzerland
关键词
HEPATITIS-C-VIRUS; REVEALS EXTENDED MICROHETEROGENEITY; ENVELOPE GLYCOPROTEIN; MONOCLONAL-ANTIBODIES; CYSTEINE RESIDUES; FUNCTIONAL-ANALYSIS; CD81; BINDING; NEUTRALIZATION; EPITOPES; E1;
D O I
10.1016/j.drudis.2014.08.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 Here, the main literature will be discussed and an alternative disulfide bridge pattern will be proposed, based on unpublished human monoclonal antibody reactivity.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.
引用
收藏
页码:1964 / 1970
页数:7
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