Literature DB >> 1706515

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

C S Park1, S F Hausdorff, C Miller.   

Abstract

A gene encoding charybdotoxin (CTX), a K+ channel blocker from scorpion venom, was designed, synthesized, and expressed as a cleavable fusion protein in Escherichia coli. A sequence-specific protease, factor Xa, was used to cleave the fusion protein and thus release the toxin peptide. The recombinant toxin was purified, oxidized to form disulfide bonds, and treated to form N-terminal pyroglutamate. Recombinant CTX is identical to the native venom CTX with respect to high-performance liquid chromatography mobility, amino acid composition, and N-terminal modification. With single Ca2(+)-activated K+ channels as an assay system, recombinant CTX shows blocking and dissociation kinetics identical to the native venom toxin. The synthetic gene and high-level expression of functionally active CTX make it possible to study the fundamental mechanism of the toxin-ion channel interaction.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1706515      PMCID: PMC51165          DOI: 10.1073/pnas.88.6.2046

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  24 in total

1.  A family of calcium-dependent potassium channels from rat brain.

Authors:  P H Reinhart; S Chung; I B Levitan
Journal:  Neuron       Date:  1989-01       Impact factor: 17.173

2.  Molecular structure of charybdotoxin, a pore-directed inhibitor of potassium ion channels.

Authors:  W Massefski; A G Redfield; D R Hare; C Miller
Journal:  Science       Date:  1990-08-03       Impact factor: 47.728

3.  Identification of two toxins from scorpion (Leiurus quinquestriatus) venom which block distinct classes of calcium-activated potassium channel.

Authors:  N A Castle; P N Strong
Journal:  FEBS Lett       Date:  1986-12-01       Impact factor: 4.124

4.  Charybdotoxin, a protein inhibitor of single Ca2+-activated K+ channels from mammalian skeletal muscle.

Authors:  C Miller; E Moczydlowski; R Latorre; M Phillips
Journal:  Nature       Date:  1985 Jan 24-30       Impact factor: 49.962

5.  Purification of charybdotoxin, a specific inhibitor of the high-conductance Ca2+-activated K+ channel.

Authors:  C Smith; M Phillips; C Miller
Journal:  J Biol Chem       Date:  1986-11-05       Impact factor: 5.157

6.  Charybdotoxin blocks with high affinity the Ca-activated K+ channel of Hb A and Hb S red cells: individual differences in the number of channels.

Authors:  D Wolff; X Cecchi; A Spalvins; M Canessa
Journal:  J Membr Biol       Date:  1988-12       Impact factor: 1.843

7.  Cloning and expression of a synthetic gene for Cerebratulus lacteus neurotoxin B-IV.

Authors:  M L Howell; K M Blumenthal
Journal:  J Biol Chem       Date:  1989-09-15       Impact factor: 5.157

8.  Purification, sequence, and model structure of charybdotoxin, a potent selective inhibitor of calcium-activated potassium channels.

Authors:  G Gimenez-Gallego; M A Navia; J P Reuben; G M Katz; G J Kaczorowski; M L Garcia
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

9.  Charybdotoxin selectively blocks small Ca-activated K channels in Aplysia neurons.

Authors:  A Hermann; C Erxleben
Journal:  J Gen Physiol       Date:  1987-07       Impact factor: 4.086

10.  Mechanism of charybdotoxin block of the high-conductance, Ca2+-activated K+ channel.

Authors:  R MacKinnon; C Miller
Journal:  J Gen Physiol       Date:  1988-03       Impact factor: 4.086

View more
  24 in total

1.  Recombinant production and solution structure of PcTx1, the specific peptide inhibitor of ASIC1a proton-gated cation channels.

Authors:  Pierre Escoubas; Cédric Bernard; Gérard Lambeau; Michel Lazdunski; Hervé Darbon
Journal:  Protein Sci       Date:  2003-07       Impact factor: 6.725

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.  Mapping hydrophobic residues of the interaction surface of charybdotoxin.

Authors:  P Stampe; L Kolmakova-Partensky; C Miller
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

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.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

6.  A designer ligand specific for Kv1.3 channels from a scorpion neurotoxin-based library.

Authors:  Zoltan Takacs; Megan Toups; Astrid Kollewe; Erik Johnson; Luis G Cuello; Gregory Driessens; Matthew Biancalana; Akiko Koide; Cristiano G Ponte; Eduardo Perozo; Thomas F Gajewski; Guilherme Suarez-Kurtz; Shohei Koide; Steve A N Goldstein
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-10       Impact factor: 11.205

7.  Electrostatic distance geometry in a K+ channel vestibule.

Authors:  M Stocker; C Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-27       Impact factor: 11.205

Review 8.  High-conductance calcium-activated potassium channels; structure, pharmacology, and function.

Authors:  G J Kaczorowski; H G Knaus; R J Leonard; O B McManus; M L Garcia
Journal:  J Bioenerg Biomembr       Date:  1996-06       Impact factor: 2.945

9.  Calcium-dependent gating of MthK, a prokaryotic potassium channel.

Authors:  Brittany Zadek; Crina M Nimigean
Journal:  J Gen Physiol       Date:  2006-06       Impact factor: 4.086

10.  BmTx3, a scorpion toxin with two putative functional faces separately active on A-type K+ and HERG currents.

Authors:  Isabelle Huys; Chen-Qi Xu; Cheng-Zhong Wang; Hélène Vacher; Marie-France Martin-Eauclaire; Cheng-Wu Chi; Jan Tytgat
Journal:  Biochem J       Date:  2004-03-15       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.