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PMID: 15155739 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Characteristic interactions with phosphatidylinositol 4,5-bisphosphate determine regulation of kir channels by diverse modulators.

The Journal of biological chemistry ·Vol. 279 ·No. 36 ·2004-09-03 ·Pages 37271-81

Du X, Zhang H, Lopes C, Mirshahi T, Rohacs T, Logothetis DE

Abstract

The activity of specific inwardly rectifying potassium (Kir) channels is regulated by any of a number of different modulators, such as protein kinase C, G(q) -coupled receptor stimulation, pH, intracellular Mg(2+) or the betagamma-subunits of G proteins. Phosphatidylinositol 4,5-bisphosphate (PIP(2)) is an essential factor for maintenance of the activity of all Kir channels. Here, we demonstrate that the strength of channel-PIP(2) interactions determines the sensitivity of Kir channels to regulation by the various modulators. Furthermore, our results suggest that differences among Kir channels in their specific regulation by a given modulator may reflect differences in their apparent affinity of interactions with PIP(2).

MeSH Terms
Animals DNA, Complementary ErbB Receptors/metabolism Mutagenesis, Site-Directed Phosphatidylinositol 4,5-Diphosphate/metabolism Potassium Channels, Inwardly Rectifying/chemistry,genetics,metabolism Xenopus laevis
Chemicals
DNA, Complementary KCNJ4 protein, human Phosphatidylinositol 4,5-Diphosphate Potassium Channels, Inwardly Rectifying ErbB Receptors
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Du Xiaona
Department of Pharmacology, Hebei Medical University, Shijiazhuang, China.
Zhang Hailin
Lopes Coeli
Mirshahi Tooraj
Rohacs Tibor
Logothetis Diomedes E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2004-09-03
Epub
2004-00-20
Pages
37271-81
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL59949 · United States
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