T-Cell inactivation and immunosuppressive activity induced by HIV gp41 via novel interacting motif

Itai Bloch, Francisco J. Quintana, Doron Gerber, Tomer Cohen, Irun R. Cohen, Yechiel Shai

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Fusion peptide (FP) of the HIV gp41 molecule inserts into the T cell membrane during virus-cell fusion. FP also blocks the TCR/CD3 interaction needed for antigen-triggered T cell activation. Here we used in vitro (fluorescence and immunoprecipitation), in vivo (T cell mediated autoimmune disease adjuvant arthritis), and in silico methods to identify the FP-TCR novel interaction motif: the α-helical transmembrane domain (TMD) of the TCR α chain, and the β-sheet 5-13 region of the 16 N-terminal aa of FP (FP 1-16). Deciphering the molecular mechanism of the immunosuppressive activity of FP provides a new potential target to overcome the immunosuppressant activity of HIV, and in addition a tool for down-regulating immune mediated inflammation.

Original languageEnglish
Pages (from-to)393-401
Number of pages9
JournalFASEB Journal
Volume21
Issue number2
DOIs
StatePublished - Feb 2007
Externally publishedYes

Keywords

  • Membrane proteins
  • Peptide-membrane interaction
  • Protein-membrane interaction
  • Recognition within membranes
  • Transmembrane domain

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