| Literature DB >> 29870724 |
Bruce J Mayer1, Ji Yu2.
Abstract
Signal transduction systems based on tyrosine phosphorylation are central to cell-cell communication in multicellular organisms. Typically, in such a system, the signal is initiated by activating tyrosine kinases associated with transmembrane receptors, which induces tyrosine phosphorylation of the receptor and/or associated proteins. The phosphorylated tyrosines then serve as docking sites for the binding of various downstream effector proteins. It has long been observed that the cooperative association of the receptors and effectors produces higher-order protein assemblies (clusters) following signal activation in virtually all phosphotyrosine signal transduction systems. However, mechanistic studies on how such clustering processes affect signal transduction outcomes have only emerged recently. Here we review current progress in decoding the biophysical consequences of clustering on the behavior of the system, and how clustering affects how these receptors process information.Entities:
Keywords: multi-protein complex; signal transduction
Mesh:
Substances:
Year: 2018 PMID: 29870724 PMCID: PMC6195463 DOI: 10.1016/j.jmb.2018.05.040
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469