Role of HIV membrane in neutralization by two broadly neutralizing antibodies

SM Alam, M Morelli, SM Dennison… - Proceedings of the …, 2009 - National Acad Sciences
SM Alam, M Morelli, SM Dennison, HX Liao, R Zhang, SM Xia, S Rits-Volloch, L Sun…
Proceedings of the National Academy of Sciences, 2009National Acad Sciences
Induction of effective antibody responses against HIV-1 infection remains an elusive goal for
vaccine development. Progress may require in-depth understanding of the molecular
mechanisms of neutralization by monoclonal antibodies. We have analyzed the molecular
actions of two rare, broadly neutralizing, human monoclonal antibodies, 4E10 and 2F5,
which target the transiently exposed epitopes in the membrane proximal external region
(MPER) of HIV-1 gp41 envelope during viral entry. Both have long CDR H3 loops with a …
Induction of effective antibody responses against HIV-1 infection remains an elusive goal for vaccine development. Progress may require in-depth understanding of the molecular mechanisms of neutralization by monoclonal antibodies. We have analyzed the molecular actions of two rare, broadly neutralizing, human monoclonal antibodies, 4E10 and 2F5, which target the transiently exposed epitopes in the membrane proximal external region (MPER) of HIV-1 gp41 envelope during viral entry. Both have long CDR H3 loops with a hydrophobic surface facing away from the peptide epitope. We find that the hydrophobic residues of 4E10 mediate a reversible attachment to the viral membrane and that they are essential for neutralization, but not for interaction with gp41. We propose that these antibodies associate with the viral membrane in a required first step and are thereby poised to capture the transient gp41 fusion intermediate. These results bear directly on strategies for rational design of HIV-1 envelope immunogens.
National Acad Sciences