Abstract
The T cell antigen receptor (TCRCD3) is a multi-subunit complex responsible for triggering an adaptive immune response. It shows high specificity and sensitivity while having a low affinity for the ligand. Furthermore, T cells respond to antigen over a wide concentration range. The stoichiometry and architecture of TCR-CD3 in the membrane have been under intense scrutiny because they might be key to explaining its paradoxical properties. This review highlights new evidence that TCR-CD3 is found on intact, unstimulated T cells in monovalent (one ligand-binding site per receptor) as well as in several distinct multivalent forms. This is in contrast to the TCR-CD3 stoichiometries determined by several biochemical means, but these data can be explained by the effects of different detergents on the integrity of the receptor. Here, we discuss a model in which the multivalent receptors are important for the detection of low concentrations of ligand, and therefore confer sensitivity, whereas the co-expressed monovalent TCR-CD3s allow a wide dynamic range.
Translated title of the contribution | T cell receptor nanocomplexes: Cooperating clusters |
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Original language | Spanish |
Pages (from-to) | 727-742 |
Number of pages | 16 |
Journal | Anales de la Real Academia Nacional de Farmacia |
Volume | 74 |
Issue number | 4 |
Publication status | Published - 1 Dec 2008 |
Keywords
- Conformational change
- Signal transduction
- Stoichiometry
- T cell antigen receptor
- Transmembrane interactions
ASJC Scopus subject areas
- Molecular Biology
- Pharmaceutical Science
- Cell Biology
- Pharmacology (medical)