2M36

Solution structure of the insecticidal spider-venom peptide Aps III

2M36 の概要

• エントリーDOI: 10.2210/pdb2m36/pdb
• NMR情報: BMRB: 18946
• 分子名称: U2-cyrtautoxin-As1a (1 entity in total)
• 機能のキーワード: asp iii, mu-cutx-as1a, inhibitor cystine knot, voltage-gated sodium channel, insect toxin, toxin
• 由来する生物種: Apomastus schlingeri (Trap-door spider)
• 細胞内の位置: Secreted: P49268
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 3859.33

構造登録者

King, G.F.,Bende, N.S.,Mobli, M. (登録日: 2013-01-10, 公開日: 2013-03-27, 最終更新日: 2023-06-14)

主引用文献

Bende, N.S.,Kang, E.,Herzig, V.,Bosmans, F.,Nicholson, G.M.,Mobli, M.,King, G.F.
The insecticidal neurotoxin Aps III is an atypical knottin peptide that potently blocks insect voltage-gated sodium channels.
Biochem Pharmacol, 85:1542-1554, 2013

PubMed Abstract: One of the most potent insecticidal venom peptides described to date is Aps III from the venom of the trapdoor spider Apomastus schlingeri. Aps III is highly neurotoxic to lepidopteran crop pests, making it a promising candidate for bioinsecticide development. However, its disulfide-connectivity, three-dimensional structure, and mode of action have not been determined. Here we show that recombinant Aps III (rAps III) is an atypical knottin peptide; three of the disulfide bridges form a classical inhibitor cystine knot motif while the fourth disulfide acts as a molecular staple that restricts the flexibility of an unusually large β hairpin loop that often houses the pharmacophore in this class of toxins. We demonstrate that the irreversible paralysis induced in insects by rAps III results from a potent block of insect voltage-gated sodium channels. Channel block by rAps III is voltage-independent insofar as it occurs without significant alteration in the voltage-dependence of channel activation or steady-state inactivation. Thus, rAps III appears to be a pore blocker that plugs the outer vestibule of insect voltage-gated sodium channels. This mechanism of action contrasts strikingly with virtually all other sodium channel modulators isolated from spider venoms that act as gating modifiers by interacting with one or more of the four voltage-sensing domains of the channel.

PubMed: 23473802
DOI: 10.1016/j.bcp.2013.02.030

実験手法

SOLUTION NMR