Two new classes of conopeptides inhibit the α1-adrenoceptor and noradrenaline transporter

被引:204
作者
Sharpe, IA
Gehrmann, J
Loughnan, ML
Thomas, L
Adams, DA
Atkins, A
Palant, E
Craik, DJ
Adams, DJ
Alewood, PF
Lewis, RJ [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Sch Biomed Sci, Dept Physiol & Pharmacol, Brisbane, Qld 4072, Australia
[3] Xenome Ltd, Brisbane, Qld 4068, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1038/nn0901-902
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cone snails use venom containing a cocktail of peptides ('conopeptides') to capture their prey. Many of these peptides also target mammalian receptors, often with exquisite selectivity. Here we report the discovery of two new classes of conopeptides. One class targets alpha (1)-adrenoceptors (rho -TIA from the fish-hunting Conus tulipa), and the second class targets the neuronal noradrenaline transporter (chi -MrIA and chi -MrIB from the mollusk-hunting C. marmoreus). rho -TIA and chi -MrIA selectively modulate these important membrane-bound proteins. Both peptides act as reversible non-competitive inhibitors and provide alternative avenues for the identification of inhibitor drugs.
引用
收藏
页码:902 / 907
页数:6
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