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Interactions of CD4 with MHC class II molecules, T cell receptors and p56lck

  • Dario A.A. Vignali
  • , Carolyn Doyle
  • , Michael S. Kinch
  • , Jaekyoon Shin
  • , Jack L. Strominger
  • Harvard University
  • Duke University

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

CD4 and CD8 are members of the immunoglobulin supergene family of proteins, and function as co- receptors with the T cell receptor (TCR) in binding MHC class II or class I molecules, respectively. Within this multimene complex, CD4 interacts with three distinct ligands. CD4 interacts through its D1 and D2 domains with MHC class II proteins, through its D3 and D4 domains with T cell receptors, and through its cytoplasmic tail with p56lck, a irf-related, protein tyrosine kinase. Each of these interactions is important in the function of CD4 and will be discussed in turn.

Original languageEnglish
Pages (from-to)13-24
Number of pages12
JournalPhilosophical Transactions of the Royal Society B: Biological Sciences
Volume342
Issue number1299
DOIs
StatePublished - Oct 1 1993

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