Publications

A potent and broad neutralizing antibody recognizes and penetrates the HIV glycan shield.

Author(s): Pejchal R,  Doores KJ,  Walker LM,  Khayat R,  Huang PS,  Wang SK,  Stanfield RL,  Julien JP,  Ramos A,  Crispin M,  Depetris R,  Katpally U,  Marozsan A,  Cupo A,  Maloveste S,  Liu Y,  McBride R,  Ito Y,  Sanders RW,  Ogohara C,  Paulson JC,  Feizi T,  Scanlan CN,  Wong CH,  Moore JP,  Olson WC,  Ward AB,  Poignard P,  Schief WR,  Burton DR,  Wilson IA

Journal: Science

Date: 2011 Nov 25

Major Program(s) or Research Group(s): GLYCO

PubMed ID: 21998254

PMC ID: PMC3280215

Abstract: The HIV envelope (Env) protein gp120 is protected from antibody recognition by a dense glycan shield. However, several of the recently identified PGT broadly neutralizing antibodies appear to interact directly with the HIV glycan coat. Crystal structures of antigen-binding fragments (Fabs) PGT 127 and 128 with Man(9) at 1.65 and 1.29 angstrom resolution, respectively, and glycan binding data delineate a specific high mannose-binding site. Fab PGT 128 complexed with a fully glycosylated gp120 outer domain at 3.25 angstroms reveals that the antibody penetrates the glycan shield and recognizes two conserved glycans as well as a short β-strand segment of the gp120 V3 loop, accounting for its high binding affinity and broad specificity. Furthermore, our data suggest that the high neutralization potency of PGT 127 and 128 immunoglobulin Gs may be mediated by cross-linking Env trimers on the viral surface.