Simulation of receptor triggering by kinetic segregation shows role of oligomers and close contacts.
Ontology highlight
ABSTRACT: The activation of T cells, key players of the immune system, involves local evacuation of phosphatase CD45 from a region of the T cell's surface, segregating it from the T cell receptor. What drives this evacuation? In the presence of antigen, what ensures evacuation happens in the subsecond timescales necessary to initiate signaling? In the absence of antigen, what mechanisms ensure that evacuation does not happen spontaneously, which could cause signaling errors? Phenomena known to influence spatial organization of CD45 or similar surface molecules include diffusive motion in the lipid bilayer, oligomerization reactions, and mechanical compression against a nearby surface, such as that of the cell presenting the antigen. Computer simulations can investigate hypothesized spatiotemporal me
SUBMITTER: Taylor R
PROVIDER: S-EPMC9117938 | biostudies-literature | 2022 May
REPOSITORIES: biostudies-literature
ACCESS DATA