Germline humanization of a non-human primate antibody that neutralizes the anthrax toxin, by in vitro and in silico engineering

T Pelat, H Bedouelle, A R Rees, Susan Crennell, M P Lefranc, P Thullier

Research output: Contribution to journalArticle

65 Citations (Scopus)

Abstract

Fab 35PA(83) is an antibody fragment of non-human primate origin that neutralizes the anthrax lethal toxin. Human antibodies are usually preferred when clinical use is envisioned, even though their framework regions (FR) may carry mutations introduced during affinity maturation. These hypermutations can be immunogenic and therefore FR that are encoded by human germline genes, encountered in IgMs and thus part of the "self" proteins, are preferable. Accordingly, the proportion of FR residues in 35PA83 that were encoded by human V and J germline genes, i.e. the germinality index (GI) of 35PA(83), was increased in a multistep cumulative approach. In a first step, the FR1 and FR4 residues of 35PA(83) were changed simultaneously into their counterparts coded by 35PA(83)'s closest human germline genes, without prior modelling. The resulting derivative of 35PA83 had the same affinity as its parental Fab. In a second step, the 3D structures of this first 35PA83 derivative, carrying the same type of residue changes but in the FR2 and FR3 regions, were modelled in silico from sequences. Some of the changes in FR2 or FR3 modified the predicted peptide backbone. The changes that did not seem to alter the structure were introduced simultaneously in the Fab by an in vitro method and resulted in a loss of reactivity, which could however be fully restored by a single point mutation. The final 35PA(83) derivative had a GI higher than that of a fully human Fab, which had neutralization properties similar to 35PA83 and which was used as a benchmark in this study.
Original languageEnglish
Pages (from-to)1400-1407
Number of pages8
JournalJournal of Molecular Biology
Volume384
Issue number5
DOIs
Publication statusPublished - 2008

Keywords

  • non-human primate
  • tri-dimensional modeling
  • antibody
  • germline genes
  • humanization

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