Literature DB >> 1673915

Electrophysiological analysis of structural aspects of voltage-dependent SR K+ channel.

M Sokabe1, M Kasai, K Nomura, K Naruse.   

Abstract

This article presents a brief review on the electrophysiological analysis of the structural aspects of the voltage-dependent SR (sarcoplasmic reticulum) K+ channel. In the first half, early attempts to determine the physical dimensions of the ion conducting mechanism such as the mouth, narrow tunnel, or ion selective filter of the channel, are reviewed. The depicted cartoon of the SR K+ channel, as an extremely short, busy district with a big mouth on each side, is quite similar to the recently-obtained reconstructed structural image of the acetylcholine receptor channel. In the latter half, we introduce our recent attempts to draw a physical image of the gating mechanism of the SR K+ channel. We examined, for example, the location of the gate and the voltage sensor, and the relationship between them. It is suggested that the gate and the sensor are connected tightly and that the sensor would be exposed to the surface of the lumen side of SR when the gate opens. Finally, the issue of substates in SR K+ channel is discussed. It is implied that the substrate-conductances reflect a partial occlusion of the pore by an intermediate-open gate.

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Year:  1991        PMID: 1673915

Source DB:  PubMed          Journal:  Comp Biochem Physiol C        ISSN: 0742-8413


  4 in total

Review 1.  Immuno-proteomic approach to excitation--contraction coupling in skeletal and cardiac muscle: molecular insights revealed by the mitsugumins.

Authors:  Noah Weisleder; Hiroshi Takeshima; Jianjie Ma
Journal:  Cell Calcium       Date:  2007-12-03       Impact factor: 6.817

Review 2.  Trimeric intracellular cation channels and sarcoplasmic/endoplasmic reticulum calcium homeostasis.

Authors:  Xinyu Zhou; Peihui Lin; Daiju Yamazaki; Ki Ho Park; Shinji Komazaki; S R Wayne Chen; Hiroshi Takeshima; Jianjie Ma
Journal:  Circ Res       Date:  2014-02-14       Impact factor: 17.367

3.  Ca2+ release by inositol 1,4,5-trisphosphate is blocked by the K(+)-channel blockers apamin and tetrapentylammonium ion, and a monoclonal antibody to a 63 kDa membrane protein: reversal of blockade by K+ ionophores nigericin and valinomycin and purification of the 63 kDa antibody-binding protein.

Authors:  F O'Rourke; K Soons; R Flaumenhauft; J Watras; C Baio-Larue; E Matthews; M B Feinstein
Journal:  Biochem J       Date:  1994-06-15       Impact factor: 3.857

4.  Structure-function study on a de novo synthetic hydrophobic ion channel.

Authors:  Z Qi; M Sokabe; K Donowaki; H Ishida
Journal:  Biophys J       Date:  1999-02       Impact factor: 4.033

  4 in total

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