P20A inhibits HIV-1 fusion through its electrostatic interaction with the distal region of the gp41 fusion core

摘要

We previously identified an HIV-1 fusion inhibitor P20A targeting HIV-1 gp4l 6-HB fusion core. Using alanine scanning mutagenesis, we investigated the effect of 6-HB surface residue mutations on the binding affinity between P20A and 6-HB. Substitution of positively or negatively charged residues in the distal region of 6-HB with alanines resulted in significant decrease or increase of its binding affinity to P20A, respectively. The 6-HB with E630K, D632K, or E634K mutation exhibited enhanced binding affinity with P20A, suggesting that P20A blocks HIV-1 fusion through electrostatic interaction with the positively charged residues in the distal region of the gp41 fusion core. (C) 2015 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.