Literature DB >> 2483092

Competition for block of a Ca2(+)-activated K+ channel by charybdotoxin and tetraethylammonium.

C Miller1.   

Abstract

Single high-conductance Ca2(+)-activated K+ channels were incorporated into planar lipid bilayers, and the discrete block by charybdotoxin (CTX), a protein inhibitor of this channel, was studied. In particular, the effect of externally added tetraethylammonium (TEA) on CTX blocking kinetics was investigated. TEA decreases the on-rate of CTX in exact proportion to its blocking of the single-channel current. The CTX off-rate is unaffected by TEA. The results demonstrate that TEA and CTX are mutually exclusive in their binding to the channel. Since the site of TEA binding is known to be located on the external side of the conduction pore, this result further strengthens the proposal that the CTX binding site is located in the external mouth of the channel.

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Year:  1988        PMID: 2483092     DOI: 10.1016/0896-6273(88)90157-2

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  33 in total

1.  Computational design of water-soluble analogues of the potassium channel KcsA.

Authors:  Avram M Slovic; Hidetoshi Kono; James D Lear; Jeffery G Saven; William F DeGrado
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-06       Impact factor: 11.205

2.  A point mutation in a Shaker K+ channel changes its charybdotoxin binding site from low to high affinity.

Authors:  S A Goldstein; C Miller
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

3.  Ca(2+)-activated K+ channels from an insulin-secreting cell line incorporated into planar lipid bilayers.

Authors:  Y Oosawa; S J Ashcroft; F M Ashcroft
Journal:  Diabetologia       Date:  1992-07       Impact factor: 10.122

Review 4.  Peptide toxins and small-molecule blockers of BK channels.

Authors:  Mu Yu; San-ling Liu; Pei-bei Sun; Hao Pan; Chang-lin Tian; Long-hua Zhang
Journal:  Acta Pharmacol Sin       Date:  2016-01       Impact factor: 6.150

5.  Slow inactivation in voltage gated potassium channels is insensitive to the binding of pore occluding peptide toxins.

Authors:  Carolina Oliva; Vivian González; David Naranjo
Journal:  Biophys J       Date:  2005-05-27       Impact factor: 4.033

6.  Design, synthesis, and functional expression of a gene for charybdotoxin, a peptide blocker of K+ channels.

Authors:  C S Park; S F Hausdorff; C Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-15       Impact factor: 11.205

7.  Competitive binding interaction between Zn2+ and saxitoxin in cardiac Na+ channels. Evidence for a sulfhydryl group in the Zn2+/saxitoxin binding site.

Authors:  L Schild; E Moczydlowski
Journal:  Biophys J       Date:  1991-03       Impact factor: 4.033

8.  Mechanism of block of the hERG K+ channel by the scorpion toxin CnErg1.

Authors:  Adam P Hill; M Sunde; T J Campbell; J I Vandenberg
Journal:  Biophys J       Date:  2007-03-16       Impact factor: 4.033

9.  Localization of the ergtoxin-1 receptors on the voltage sensing domain of hERG K+ channel by AFM recognition imaging.

Authors:  Lilia A Chtcheglova; Fatmahan Atalar; Ugur Ozbek; Linda Wildling; Andreas Ebner; Peter Hinterdorfer
Journal:  Pflugers Arch       Date:  2008-02-20       Impact factor: 3.657

10.  The external TEA binding site and C-type inactivation in voltage-gated potassium channels.

Authors:  Payam Andalib; Joseph F Consiglio; Josef G Trapani; Stephen J Korn
Journal:  Biophys J       Date:  2004-08-23       Impact factor: 4.033

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