Sequence and Structural Convergence of Broad and Potent HIV Antibodies That Mimic CD4 Binding

Johannes F. Scheid(Charité - Universitätsmedizin Berlin), Hugo Mouquet(Rockefeller University), Beatrix Ueberheide(Rockefeller University), Ron Diskin(California Institute of Technology), Florian Klein(Rockefeller University), Thiago Y. Oliveira(Rockefeller University), John Pietzsch(Freie Universität Berlin), David Fenyö(Rockefeller University), Alexander Abadir(Rockefeller University), Klara Velinzon(Rockefeller University), Arlene Hurley(Rockefeller University Hospital), Sunnie Myung(Rockefeller University), Farid Boulad(Memorial Sloan Kettering Cancer Center), Pascal Poignard(Scripps Research Institute), Dennis R. Burton(Scripps Research Institute), Florencia Pereyra(Harvard University), David D. Ho(Howard Hughes Medical Institute), Bruce D. Walker(Howard Hughes Medical Institute), Michael S. Seaman(Beth Israel Deaconess Medical Center), Pamela J. Björkman(California Institute of Technology), Brian T. Chait(Rockefeller University), Michel C. Nussenzweig(Howard Hughes Medical Institute)
Science
July 14, 2011
Cited by 1,178Open Access
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Abstract

Passive transfer of broadly neutralizing HIV antibodies can prevent infection, which suggests that vaccines that elicit such antibodies would be protective. Thus far, however, few broadly neutralizing HIV antibodies that occur naturally have been characterized. To determine whether these antibodies are part of a larger group of related molecules, we cloned 576 new HIV antibodies from four unrelated individuals. All four individuals produced expanded clones of potent broadly neutralizing CD4-binding-site antibodies that mimic binding to CD4. Despite extensive hypermutation, the new antibodies shared a consensus sequence of 68 immunoglobulin H (IgH) chain amino acids and arise independently from two related IgH genes. Comparison of the crystal structure of one of the antibodies to the broadly neutralizing antibody VRC01 revealed conservation of the contacts to the HIV spike.


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