Multiple PIP2 binding sites in Kir-2.1 inwardly rectifying potassium channels

被引:111
作者
Soom, M
Schönherr, R
Kubo, Y
Kirsch, C
Klinger, R
Heinemann, SH
机构
[1] Univ Jena, Fac Med, D-07747 Jena, Germany
[2] Tokyo Med & Dent Univ, Grad Sch, Dept Physiol, Bunkyo Ku, Tokyo, Japan
[3] Tokyo Med & Dent Univ, Fac Med, Bunkyo Ku, Tokyo 113, Japan
[4] Univ Jena, Fac Med, Inst Biochem, D-07743 Jena, Germany
关键词
inward rectifier potassium channel; voltage clamp; Kir2.1; lipid-protein interaction; binding assay; phosphatidylinositol-4,5-bisyhosphate;
D O I
10.1016/S0014-5793(01)02136-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inwardly rectifying potassium channels require binding of phosphatidylinositol-4,5-bisphosphate (PIP2) for channel activity. Three independent sites (aa 175-206, aa 207-246, aa 324-365) were located in the C-terminal domain of Kir2.1 channels by assaying the binding of overlapping fragments to PIP2 containing liposomes. Mutations in the first site, which abolished channel activity, reduced PIP2 binding of this fragment but not of the complete C-terminus, Point mutations in the third site also reduced both, channel activity and PIP2 binding of this segment. The relevance of the third PIP2 binding site provides a basis for the understanding of constitutively active Kir2 channels. (C) 2001 Federation of European Biochemical Societies, Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:49 / 53
页数:5
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