Rational Engineering of a Human Anti-Dengue Antibody through Experimentally Validated Computational Docking

被引:29
作者
Simonelli, Luca [1 ]
Pedotti, Mattia [1 ]
Beltramello, Martina [1 ]
Livoti, Elsa [1 ]
Calzolai, Luigi [2 ]
Sallusto, Federica [1 ]
Lanzavecchia, Antonio [1 ,3 ]
Varani, Luca [1 ]
机构
[1] Biomed Res Inst, Bellinzona, Switzerland
[2] Commiss European Communities, Joint Res Ctr, Inst Hlth & Consumer Protect, I-21020 Ispra, Italy
[3] ETH, Inst Microbiol, CH-8092 Zurich, Switzerland
来源
PLOS ONE | 2013年 / 8卷 / 02期
关键词
PROTEIN-PROTEIN DOCKING; VIRUS ENVELOPE PROTEIN; DOMAIN-III; NEUTRALIZING ANTIBODY; CROSS-REACTIVITY; E-GLYCOPROTEIN; BINDING; DESIGN; ASSIGNMENTS; REVEALS;
D O I
10.1371/journal.pone.0055561
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibodies play an increasing pivotal role in both basic research and the biopharmaceutical sector, therefore technology for characterizing and improving their properties through rational engineering is desirable. This is a difficult task thought to require high-resolution x-ray structures, which are not always available. We, instead, use a combination of solution NMR epitope mapping and computational docking to investigate the structure of a human antibody in complex with the four Dengue virus serotypes. Analysis of the resulting models allows us to design several antibody mutants altering its properties in a predictable manner, changing its binding selectivity and ultimately improving its ability to neutralize the virus by up to 40 fold. The successful rational design of antibody mutants is a testament to the accuracy achievable by combining experimental NMR epitope mapping with computational docking and to the possibility of applying it to study antibody/pathogen interactions.
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页数:11
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