| Literature DB >> 31867822 |
Lela Jackson1, Androniqi Qifti1, Katherine M Pearce1, Suzanne Scarlata1.
Abstract
Some proteins can serve multiple functions depending on different cellular conditions. An example of a bifunctional protein is inositide-specific mammalian phospholipase Cβ (PLCβ). PLCβ is activated by G proteins in response to hormones and neurotransmitters to increase intracellular calcium. Recently, alternate cellular function(s) of PLCβ have become uncovered. However, the conditions that allow these different functions to be operative are unclear. Like many mammalian proteins, PLCβ has a conserved catalytic core along with several regulatory domains. These domains modulate the intensity and duration of calcium signals in response to external sensory information, and allow this enzyme to inhibit protein translation in a noncatalytic manner. In this review, we first describe PLCβ's cellular functions and regulation of the switching between these functions, and then discuss the thermodynamic considerations that offer insight into how cells manage multiple and competitive associations allowing them to rapidly shift between functional states.Entities:
Keywords: G proteins; RNA-induced silencing; bifunctional enzymes; calcium signaling; cell localization; cell regulation; phospholipaseC
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Year: 2019 PMID: 31867822 PMCID: PMC7255524 DOI: 10.1002/pro.3809
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725