Year: 2026
Type: article
Abstract: The disordered adapter protein linker for activation of T cells (LAT) propagates T cell receptor signaling. To interrogate how LAT coordinates multiple downstream pathways, we developed a single-cell screening approach, identifying widespread functional segments including protein interaction motifs and blocks of negative charge. Regardless of their position in LAT, individual segments generally conferred defects across all downstream signaling pathways. To understand the underlying mechanism, we used molecular biology, computational modeling, and imaging to demonstrate that disruption of LAT interaction with a single partner protein indirectly disrupts other partner interactions, likely through the dual roles of these proteins as effectors of downstream signaling and bridging factors between LAT molecules. Overall, we describe an extendable approach for interrogating sequence-function relationships for proteins with complex activities.
Source: Science
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: green
Funders: U.S. Department of Agriculture, Bill and Melinda Gates Foundation, Helen Hay Whitney Foundation, Ragon Institute of MGH, MIT and Harvard, Broad Institute, Novo Nordisk, Novo Nordisk Fonden, National Institutes of Health, Agricultural Research Service, Klarman Cell Observatory, Broad Institute, National Institute on Drug Abuse, National Institute of Allergy and Infectious Diseases
OpenAlex ID: W7159668175
