Literature DB >> 10553073

Amino acids specifying MHC class preference in TCR V alpha 2 regions.

M Correia-Neves1, C Waltzinger, J M Wurtz, C Benoist, D Mathis.   

Abstract

Some TCR variable regions are preferentially expressed in CD4+ or CD8+ T cells, reflecting a predilection for interacting with MHC class II or class I molecules. The molecular basis for MHC class bias has been studied previously, in particular for V alpha 3 family members, pointing to a dominant role for two amino acid positions in complementary-determining regions (CDRs) 1 and 2. We have evaluated the generality of these findings by examining the MHC class bias of V alpha 2 family members, an attractive system because it shows more variability within the CDR1 and -2, exhibits variation in the framework regions, and includes a member for which the crystal structure has been determined. We find that preferential recognition of MHC class I or II molecules does not always depend on residues at the same positions of CDR1 and -2; rules for one family may be reversed in another. Instead, there are multiple influences exerted by various CDR1/2 positions as well as the CDR3s of both the TCR alpha- and TCR beta-chains.

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Year:  1999        PMID: 10553073

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  7 in total

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Review 4.  T cell receptor binding kinetics and special role of Valpha in T cell development and activation.

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Review 5.  TCR-MHC docking orientation: natural selection, or thymic selection?

Authors:  Edward J Collins; David S Riddle
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6.  T cell receptor gene rearrangement lineage analysis reveals clues for the origin of highly restricted antigen-specific repertoires.

Authors:  Abdelbasset Hamrouni; Anne Aublin; Philippe Guillaume; Janet L Maryanski
Journal:  J Exp Med       Date:  2003-03-03       Impact factor: 14.307

7.  Inherent reactivity of unselected TCR repertoires to peptide-MHC molecules.

Authors:  S Harsha Krovi; John W Kappler; Philippa Marrack; Laurent Gapin
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-30       Impact factor: 11.205

  7 in total

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