TY - JOUR
T1 - New "Birtoxin analogs" from Androctonus australis venom
AU - Martin-Eauclaire, Marie-France
AU - Ceard, Brigitte
AU - Bosmans, Frank
AU - Rosso, Jean-Pierre
AU - Tytgat, Jan
AU - Bougis, Pierre E
PY - 2005/7/29
Y1 - 2005/7/29
N2 - From the venom of the scorpion Androctonus australis, we have isolated a new bioactive polypeptide termed AaBTX-L1. When tested on the insect voltage-gated Na(+) channel (para) of the fruit fly, this toxin was able to induce a clear shift in activation (V(1/2)), resulting in the opening of the channel at more negative membrane potentials. Furthermore, AaBTX-L1 was totally devoid of toxicity when injected into mice intracerebroventricularly and did not compete with radiolabeled voltage-gated K(+) and Na(+) channel toxins in binding experiments on rat brain synaptosomes. Using its N-terminal amino acid sequence to design degenerate primers, several clones were amplified by PCR from the A. australis venom gland cDNA library. As a consequence, seven full oligonucleotide sequences encoding "long-chain" polypeptides with only three disulfide bridges have been cloned for the first time and are described here. Remarkably, they share high similarity with the anti-insect toxin Birtoxin from Parabuthus transvaalicus.
AB - From the venom of the scorpion Androctonus australis, we have isolated a new bioactive polypeptide termed AaBTX-L1. When tested on the insect voltage-gated Na(+) channel (para) of the fruit fly, this toxin was able to induce a clear shift in activation (V(1/2)), resulting in the opening of the channel at more negative membrane potentials. Furthermore, AaBTX-L1 was totally devoid of toxicity when injected into mice intracerebroventricularly and did not compete with radiolabeled voltage-gated K(+) and Na(+) channel toxins in binding experiments on rat brain synaptosomes. Using its N-terminal amino acid sequence to design degenerate primers, several clones were amplified by PCR from the A. australis venom gland cDNA library. As a consequence, seven full oligonucleotide sequences encoding "long-chain" polypeptides with only three disulfide bridges have been cloned for the first time and are described here. Remarkably, they share high similarity with the anti-insect toxin Birtoxin from Parabuthus transvaalicus.
KW - Amino Acid Sequence
KW - Animals
KW - Cells, Cultured
KW - Dose-Response Relationship, Drug
KW - Membrane Potentials/drug effects
KW - Mice
KW - Molecular Sequence Data
KW - Oocytes/drug effects
KW - Rats
KW - Scorpion Venoms/chemistry
KW - Scorpions/metabolism
KW - Sequence Homology, Amino Acid
KW - Species Specificity
KW - Survival Analysis
KW - Synaptosomes/metabolism
KW - Xenopus laevis
U2 - 10.1016/j.bbrc.2005.05.148
DO - 10.1016/j.bbrc.2005.05.148
M3 - Article
C2 - 15963953
SN - 0006-291X
VL - 333
SP - 524
EP - 530
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -