Preconfiguration of the antigen-binding site during affinity maturation of a broadly neutralizing influenza virus antibody.

نویسندگان

  • Aaron G Schmidt
  • Huafeng Xu
  • Amir R Khan
  • Timothy O'Donnell
  • Surender Khurana
  • Lisa R King
  • Jody Manischewitz
  • Hana Golding
  • Pirada Suphaphiphat
  • Andrea Carfi
  • Ethan C Settembre
  • Philip R Dormitzer
  • Thomas B Kepler
  • Ruijun Zhang
  • M Anthony Moody
  • Barton F Haynes
  • Hua-Xin Liao
  • David E Shaw
  • Stephen C Harrison
چکیده

Affinity maturation refines a naive B-cell response by selecting mutations in antibody variable domains that enhance antigen binding. We describe a B-cell lineage expressing broadly neutralizing influenza virus antibodies derived from a subject immunized with the 2007 trivalent vaccine. The lineage comprises three mature antibodies, the unmutated common ancestor, and a common intermediate. Their heavy-chain complementarity determining region inserts into the conserved receptor-binding pocket of influenza HA. We show by analysis of structures, binding kinetics and long time-scale molecular dynamics simulations that antibody evolution in this lineage has rigidified the initially flexible heavy-chain complementarity determining region by two nearly independent pathways and that this preconfiguration accounts for most of the affinity gain. The results advance our understanding of strategies for developing more broadly effective influenza vaccines.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 110 1  شماره 

صفحات  -

تاریخ انتشار 2013