iScience (Sep 2021)

Focal accumulation of aromaticity at the CDRH3 loop mitigates 4E10 polyreactivity without altering its HIV neutralization profile

  • Edurne Rujas,
  • Daniel P. Leaman,
  • Sara Insausti,
  • Pablo Carravilla,
  • Miguel García-Porras,
  • Eneko Largo,
  • Izaskun Morillo,
  • Rubén Sánchez-Eugenia,
  • Lei Zhang,
  • Hong Cui,
  • Ibon Iloro,
  • Félix Elortza,
  • Jean-Philippe Julien,
  • Christian Eggeling,
  • Michael B. Zwick,
  • Jose M.M. Caaveiro,
  • José L. Nieva

Journal volume & issue
Vol. 24, no. 9
p. 102987

Abstract

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Summary: Broadly neutralizing antibodies (bnAbs) against HIV-1 are frequently associated with the presence of autoreactivity/polyreactivity, a property that can limit their use as therapeutic agents. The bnAb 4E10, targeting the conserved Membrane proximal external region (MPER) of HIV-1, displays almost pan-neutralizing activity across globally circulating HIV-1 strains but exhibits nonspecific off-target interactions with lipid membranes. The hydrophobic apex of the third complementarity-determining region of the heavy chain (CDRH3) loop, which is essential for viral neutralization, critically contributes to this detrimental effect. Here, we have replaced the aromatic/hydrophobic residues from the apex of the CDRH3 of 4E10 with a single aromatic molecule through chemical modification to generate a variant that preserves the neutralization potency and breadth of 4E10 but with reduced autoreactivity. Collectively, our study suggests that the localized accumulation of aromaticity by chemical modification provides a pathway to ameliorate the adverse effects triggered by the CDRH3 of anti-HIV-1 MPER bnAbs.

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