Department of Pharmacology, University of California Irvine, Irvine, California, United States of America.
PLoS One. 2012;7(7):e40417. doi: 10.1371/journal.pone.0040417. Epub 2012 Jul 9.
By screening extracts of venom from the Asian scorpion Buthus martensii Karsch (BmK) for their abilities to activate opioid receptors, we have identified BmK-YA, an amidated peptide containing an enkephalin-like sequence. BmK-YA is encoded by a precursor that displays a signal sequence and contains four copies of BmK-YA sequences and four of His(4)-BmK-YA, all flanked by single amino acid residues. BmK-YA and His(4)-BmK-YA are amidated and thus fulfill the characteristics expected of bioactive peptides. BmK-YA can activate mammalian opioid receptors with selectivity for the δ subtype while His(4)-BmK-YA is inactive at opioid receptors. The discovery of BmK-YA suggests that scorpion venom may represent a novel source of bioactive molecules targeting G protein-coupled receptors (GPCRs) and reveal additional insights on the evolution of the opioid precursors.
通过筛选亚洲蝎子 Buthus martensii Karsch(BmK)毒液提取物的激活阿片受体的能力,我们鉴定了 BmK-YA,这是一种含有脑啡肽样序列的酰胺化肽。BmK-YA 由一种前体编码,该前体含有一个信号序列,包含四个 BmK-YA 序列和四个 His(4)-BmK-YA 序列,均由单个氨基酸残基侧翼。BmK-YA 和 His(4)-BmK-YA 被酰胺化,因此满足生物活性肽的预期特征。BmK-YA 可以激活哺乳动物阿片受体,对 δ 亚型具有选择性,而 His(4)-BmK-YA 在阿片受体上没有活性。BmK-YA 的发现表明,蝎子毒液可能是针对 G 蛋白偶联受体(GPCR)的生物活性分子的新来源,并揭示了阿片前体进化的更多见解。