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FEBS Lett. 1994 Dec 19;356(2-3):199-203.

A structural determinant of differential sensitivity of cloned inward rectifier K+ channels to intracellular spermine.

Author information

1
Department of Sensory Biophysics, ENT-Hospital of the University of Tübingen, Germany.

Abstract

Large subtype-specific differences in the sensitivity of cloned inward-rectifier K+ channels of the IRK1, BIR10 and ROMK1 subtype to being blocked by intracellular spermine (SPM) are described. It is shown, by site-directed mutagenesis, that the four orders of magnitude larger SPM sensitivity of BIR10 channels compared to ROMK1 channels may be explained by a difference in a single amino acid in the putative transmembrane segment TMII. This residue, a negatively charged glutamate in BIR10, is homologous to the residue in IRK1 and ROMK1 which has previously been shown to change gating properties and Mg2+ sensitivity. Differential block by physiological SPM concentrations is suggested as a major functional difference between subtypes of inward-rectifier K+ channels.

PMID:
7805837
DOI:
10.1016/0014-5793(94)01258-x
[Indexed for MEDLINE]
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