Biology of heterotrimeric G-protein signaling

Authors
Citation
Ra. Forse, Biology of heterotrimeric G-protein signaling, CRIT CARE M, 28(4), 2000, pp. N53-N59
Citations number
54
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
28
Issue
4
Year of publication
2000
Supplement
S
Pages
N53 - N59
Database
ISI
SICI code
0090-3493(200004)28:4<N53:BOHGS>2.0.ZU;2-W
Abstract
The G proteins are components of a complex membrane signaling system design ed to modulate extracellular signals as they are transmitted into the cell. The principal components are the receptor, the G proteins including the al pha, beta, gamma subunits and the effector. Associated with these molecules are several molecular processes by which the signal is transmitted, and re gulated including desensitization. Molecules such as arrestin, the RGS (reg ulators of the G-protein signaling) as well as downstream kinases associate d with cyclic AMP are key to regulating the G protein signal. Membrane lipi ds are key for both anchoring this signal system to the plasma membrane but also in defining the signaling process. Through understanding the biology of the signal system, a number of diseases have been linked to dysfunction of the G protein system. It is clear that this important membrane signal sy stem will become the target for more intense investigation and pharmacologi c manipulation to treat critical illness.