Omega-grammotoxin SIA
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[edit] Summary
Omega-grammotoxin SIA is a protein toxin that inhibits P, Q and N voltage-gated calcium channels (Ca 2+ channels) in neurons.
[edit] Source
The source of omega-grammotoxin SIA is the venom of a tarantula spider (Grammostola spatulate).
[edit] Chemistry
Amino Acid Sequence:
Asp-Cys-Val-Arg-Phe-Trp-Gly-Lys-Cys-Ser-Gln-Thr-Ser-Asp-Cys-Cys-Pro-His-Leu-Ala-Cys-Lys-Ser-Lys-Trp-Pro-Arg-Asn-Ile-Cys-Val-Trp-Asp-Gly-Ser-Val (1)
Molecular Formula: C177H268N52O50S6 (1)
Omega-grammotoxin SIA can be purified from Grammostola spatulata venom by reverse phase high performance liquid chromatography.(2)
[edit] Target
Omega-Grammotoxin SIA is a 36 amino acid residue protein toxin from spider venom that inhibits P, Q and N-type voltage-gated calcium channels in neurons. It binds to the channels with high affinity (if closed). It also binds to potassium channels but with lower affinity than to the calcium channels.(3) The toxin binding site has high affinity when channels are in closed states and low affinity when channels are activated. (4)
[edit] Mode of action
It is believed that omega-grammotoxin SIA inhibits channel function by binding with high affinity to closed, resting states of the channel and that bound toxin makes it more difficult for channels to be opened by depolarization, so much larger depolarizations are required for channel activation. (4)
[edit] Reference
(1) http://www.sigmaaldrich.com/catalog/search/ProductDetail?ProdNo=G2795&Brand=SIGMA
(2) Lampe R.A. et al. Isolation and pharmacological characterization of omega-grammotoxin SIA, a novel peptide inhibitor of neuronal voltage-sensitive calcium channel responses. Mol Pharmacol. 1993 Aug;44(2):451-60link title
(3) Takeuchi K. et al. Solution Structure of v-Grammotoxin SIA, A Gating Modifier of P/Q and N-type Ca21 Channel. J. Mol. Biol. 2002, 321: 517–526 link title
(4) Stefan I. McDonough et al. Voltage-Dependent Inhibition of N- and P-Type Calcium Channels by the Peptide Toxin v-Grammotoxin-SIA. Molucular pharmacology, 1997 52:1095–1104.link title
