Structural mechanisms of costimulation.

Abstract:

:Recent studies have highlighted the structural requirements for T cell costimulation and have revealed unusual modes of dimerization for the cytolytic T lymphocyte-associated antigen 4 (CTLA-4) costimulatory receptor and its B7 ligands. These distinctive quaternary structures potentially endow both receptor and ligand with bivalent binding properties, which suggests a number of mechanistic features relevant to signaling. These include the potential to form a highly ordered, alternating network of CTLA-4 and B7 homodimers that may represent the organization of these molecules and their associated signaling partners within the immunological synapse. Primary sequence and structural considerations suggest that some aspects of the organizational and mechanistic features associated with the CTLA-4-B7 complexes may extend to other members of the costimulatory receptor-ligand family. An examination of the signaling mechanisms within the costimulatory receptor-ligand family provides an excellent framework to consider the general principles that are relevant to cell surface receptor-mediated signaling events.

journal_name

Nat Immunol

journal_title

Nature immunology

authors

Schwartz JC,Zhang X,Nathenson SG,Almo SC

doi

10.1038/ni0502-427

keywords:

subject

Has Abstract

pub_date

2002-05-01 00:00:00

pages

427-34

issue

5

eissn

1529-2908

issn

1529-2916

pii

ni0502-427

journal_volume

3

pub_type

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