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@ARTICLE{Lenik:943344,
author = {Lešnik, Samo and Bertalan, Éva and Bren, Urban and
Bondar, Ana-Nicoleta},
title = {{O}pioid {R}eceptors and {P}rotonation-{C}oupled {B}inding
of {O}pioid {D}rugs},
journal = {International journal of molecular sciences},
volume = {22},
number = {24},
issn = {1422-0067},
address = {Basel},
publisher = {Molecular Diversity Preservation International},
reportid = {FZJ-2023-00950},
pages = {13353 -},
year = {2021},
abstract = {Opioid receptors are G-protein-coupled receptors (GPCRs)
part of cell signaling paths of direct interest to treat
pain. Pain may associate with inflamed tissue characterized
by acidic pH. The potentially low pH at tissue targeted by
opioid drugs in pain management could impact drug binding to
the opioid receptor, because opioid drugs typically have a
protonated amino group that contributes to receptor binding,
and the functioning of GPCRs may involve protonation change.
In this review, we discuss the relationship between
structure, function, and dynamics of opioid receptors from
the perspective of the usefulness of computational studies
to evaluate protonation-coupled opioid-receptor
interactions},
cin = {IAS-5 / INM-9},
ddc = {540},
cid = {I:(DE-Juel1)IAS-5-20120330 / I:(DE-Juel1)INM-9-20140121},
pnm = {5241 - Molecular Information Processing in Cellular Systems
(POF4-524)},
pid = {G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
pubmed = {34948150},
UT = {WOS:000738602000001},
doi = {10.3390/ijms222413353},
url = {https://juser.fz-juelich.de/record/943344},
}