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@ARTICLE{Vickery:836022,
author = {Vickery, Owen N and Machtens, Jan-Philipp and Zachariae,
Ulrich},
title = {{M}embrane potentials regulating {GPCR}s: insights from
experiments and molecular dynamics simulations},
journal = {Current opinion in pharmacology},
volume = {30},
issn = {1471-4892},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {FZJ-2017-05147},
pages = {44 - 50},
year = {2016},
abstract = {G-protein coupled receptors (GPCRs) form the largest class
of membrane proteins in humans and the targets of most
present drugs. Membrane potential is one of the defining
characteristics of living cells. Recent work has shown that
the membrane voltage, and changes thereof, modulates signal
transduction and ligand binding in GPCRs. As it may allow
differential signalling patterns depending on tissue, cell
type, and the excitation status of excitable cells, GPCR
voltage sensitivity could have important implications for
their pharmacology. This review summarises recent
experimental insights on GPCR voltage regulation and the
role of molecular dynamics simulations in identifying the
structural basis of GPCR voltage-sensing. We discuss the
potential significance for drug design on GPCR targets from
excitable and non-excitable cells.},
cin = {ICS-4},
ddc = {340},
cid = {I:(DE-Juel1)ICS-4-20110106},
pnm = {551 - Functional Macromolecules and Complexes (POF3-551)},
pid = {G:(DE-HGF)POF3-551},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000386861200009},
pubmed = {pmid:27474871},
doi = {10.1016/j.coph.2016.06.011},
url = {https://juser.fz-juelich.de/record/836022},
}