
LAT: the ZAP-70 tyrosine kinase substrate that links T cell receptor to cellular activation.
Despite extensive study, several of the major components involved in T cell receptor-mediated signaling remain unidentified. Here we report the cloning of the cDNA for a highly tyrosine-phosphorylated 36-38 kDa protein, previously characterized by its association with Grb2, phospholipase C-gamma1, and the p85 subunit of phosphoinositide 3-kinase. Deduced amino acid sequence identifies a novel integral membrane protein containing multiple potential tyrosine phosphorylation sites. We show that this protein is phosphorylated by ZAP-70/Syk protein tyrosine kinases leading to recruitment of multiple signaling molecules. Its function is demonstrated by inhibition of T cell activation following overexpression of a mutant form lacking critical tyrosine residues. Therefore, we propose to name the molecule LAT-linker for activation of T cells.
Duke Scholars
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Related Subject Headings
- ZAP-70 Protein-Tyrosine Kinase
- Type C Phospholipases
- Tissue Distribution
- Syk Kinase
- Substrate Specificity
- Signal Transduction
- Sequence Homology, Amino Acid
- Receptors, Antigen, T-Cell
- Rats
- Proteins
Citation

Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- ZAP-70 Protein-Tyrosine Kinase
- Type C Phospholipases
- Tissue Distribution
- Syk Kinase
- Substrate Specificity
- Signal Transduction
- Sequence Homology, Amino Acid
- Receptors, Antigen, T-Cell
- Rats
- Proteins