1PJV

Cobatoxin 1 from Centruroides noxius Scorpion venom: Chemical Synthesis, 3-D Structure in Solution, Pharmacology and Docking on K+ channels

Summary for 1PJV

• Entry DOI: 10.2210/pdb1pjv/pdb
• Descriptor: Cobatoxin 1 (1 entity in total)
• Functional Keywords: cobatoxin 1, scorpion toxin, centuroides noxius, k+ channel, chemical synthesis, 3-d structure, 1h-nmr spectroscopy, circular dichroism, molecular modeling, docking experiment, toxin
• Cellular location: Secreted: O46028
• Total number of polymer chains: 1
• Total formula weight: 3746.42

Authors

Mosbah, A.,Jouirou, B.,Visan, V.,Grissmer, S.,El Ayeb, M.,Rochat, H.,De Waard, M.,Mabrouk, K.,Sabatier, J.M. (deposition date: 2003-06-03, release date: 2004-03-09, Last modification date: 2024-11-06)

Primary citation

Jouirou, B.,Mosbah, A.,Visan, V.,Grissmer, S.,M'Barek, S.,Fajloun, Z.,Van Rietschoten, J.,Devaux, C.,Rochat, H.,Lippens, G.,El Ayeb, M.,De Waard, M.,Mabrouk, K.,Sabatier, J.M.
Cobatoxin 1 from Centruroides noxius scorpion venom: chemical synthesis, three-dimensional structure in solution, pharmacology and docking on K+ channels.
Biochem.J., 377:37-49, 2004

PubMed Abstract: CoTX1 (cobatoxin 1) is a 32-residue toxin with three disulphide bridges that has been isolated from the venom of the Mexican scorpion Centruroides noxius Hoffmann. Here we report the chemical synthesis, disulphide bridge organization, 3-D (three-dimensional) solution structure determination, pharmacology on K+ channel subtypes (voltage-gated and Ca2+-activated) and docking-simulation experiments. An enzyme-based cleavage of the synthetic folded/oxidized CoTX1 indicated half-cystine pairs between Cys3-Cys22, Cys8-Cys27 and Cys12-Cys29. The 3-D structure of CoTX1 (solved by 1H-NMR) showed that it folds according to the common alpha/beta scaffold of scorpion toxins. In vivo, CoTX1 was lethal after intracerebroventricular injection to mice (LD50 value of 0.5 microg/mouse). In vitro, CoTX1 tested on cells expressing various voltage-gated or Ca2+-activated (IKCa1) K+ channels showed potent inhibition of currents from rat K(v)1.2 ( K(d) value of 27 nM). CoTX1 also weakly competed with 125I-labelled apamin for binding to SKCa channels (small-conductance Ca2+-activated K+ channels) on rat brain synaptosomes (IC50 value of 7.2 microM). The 3-D structure of CoTX1 was used in docking experiments which suggests a key role of Arg6 or Lys10, Arg14, Arg18, Lys21 (dyad), Ile23, Asn24, Lys28 and Tyr30 (dyad) residues of CoTX1 in its interaction with the rat K(v)1.2 channel. In addition, a [Pro7,Gln9]-CoTX1 analogue (ACoTX1) was synthesized. The two residue replacements were selected aiming to restore the RPCQ motif in order to increase peptide affinity towards SKCa channels, and to alter the CoTX1 dipole moment such that it is expected to decrease peptide activity on K(v) channels. Unexpectedly, ACoTX1 exhibited an activity similar to that of CoTX1 towards SKCa channels, while it was markedly more potent on IKCa1 and several voltage-gated K+ channels.

PubMed: 14498829
DOI: 10.1042/BJ20030977

Experimental method

SOLUTION NMR