Literature DB >> 8562075

A strongly interacting pair of residues on the contact surface of charybdotoxin and a Shaker K+ channel.

D Naranjo1, C Miller.   

Abstract

Charybdotoxin, a peptide neurotoxin of known molecular structure, blocks Shaker K+ channels by binding to a receptor at the outer opening of the ion conduction pathway. Analysis of variants of CTX at position 29 and of Shaker at position 449 shows that these two residues interact closely in the channel-toxin complex. The CTX mutation M29I leads to a slight strengthening of block when tested on Shaker-449T; the same CTX mutation weakens block 1700-fold when tested on Shaker-449F. The known position of CTX-29 on the toxin's interaction surface thus locates Shaker-449 within 5 A of the pore axis of the closed channel. All four subunits must carry the 449F mutation to produce a highly toxin-insensitive channel.

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Year:  1996        PMID: 8562075     DOI: 10.1016/s0896-6273(00)80029-x

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


  41 in total

1.  Solution structure of hpTX2, a toxin from Heteropoda venatoria spider that blocks Kv4.2 potassium channel.

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Journal:  Protein Sci       Date:  2000-11       Impact factor: 6.725

2.  Genomic organization of three novel toxins from the scorpion Buthus martensi Karsch that are active on potassium channels.

Authors:  L Dai; J J Wu; Y H Gu; Z D Lan; M H Ling; C W Chi
Journal:  Biochem J       Date:  2000-03-15       Impact factor: 3.857

3.  Mechanisms of maurotoxin action on Shaker potassium channels.

Authors:  V Avdonin; B Nolan; J M Sabatier; M De Waard; T Hoshi
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

4.  Inhibition of single Shaker K channels by kappa-conotoxin-PVIIA.

Authors:  David Naranjo
Journal:  Biophys J       Date:  2002-06       Impact factor: 4.033

5.  Modeling the structure of agitoxin in complex with the Shaker K+ channel: a computational approach based on experimental distance restraints extracted from thermodynamic mutant cycles.

Authors:  Mats A L Eriksson; Benoît Roux
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

6.  C-type inactivation involves a significant decrease in the intracellular aqueous pore volume of Kv1.4 K+ channels expressed in Xenopus oocytes.

Authors:  XueJun Jiang; Glenna C L Bett; XiaoYan Li; Vladimir E Bondarenko; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

7.  Computational simulations of interactions of scorpion toxins with the voltage-gated potassium ion channel.

Authors:  Kunqian Yu; Wei Fu; Hong Liu; Xiaomin Luo; Kai Xian Chen; Jianping Ding; Jianhua Shen; Hualiang Jiang
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

8.  Structural and functional consequences of the presence of a fourth disulfide bridge in the scorpion short toxins: solution structure of the potassium channel inhibitor HsTX1.

Authors:  P Savarin; R Romi-Lebrun; S Zinn-Justin; B Lebrun; T Nakajima; B Gilquin; A Menez
Journal:  Protein Sci       Date:  1999-12       Impact factor: 6.725

9.  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

10.  Inhibition of ClC-2 chloride channels by a peptide component or components of scorpion venom.

Authors:  C H Thompson; D M Fields; P R Olivetti; M D Fuller; Z R Zhang; J Kubanek; N A McCarty
Journal:  J Membr Biol       Date:  2005-11       Impact factor: 1.843

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