A C-type natriuretic peptide from the venom of the platypus (Ornithorhynchus anatinus): Structure and pharmacology

被引:31
作者
de Plater, GM
Martin, RL
Milburn, PJ [1 ]
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Ctr Mol Struct & Funct, Canberra, ACT 0200, Australia
[2] Australian Natl Univ, Div Bot & Zool, Canberra, ACT 0200, Australia
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY | 1998年 / 120卷 / 01期
基金
澳大利亚研究理事会;
关键词
natriuretic peptide; Ornithorhynchus; platypus; peptide sequence; smooth muscle; venom;
D O I
10.1016/S0742-8413(98)00030-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A peptide which relaxes rat uterine smooth muscle and exhibits homology with the mammalian C-type natriuretic peptide (CNP) has previously been identified in platypus (Ornithorhynchus anatinus) venom from its partial N-terminal amino acid sequence. In this study we describe the purification, detailed structure, synthesis and pharmacological characteristics of this peptide, which has been designated ovCNP-39 (Ornithorhynchus venom C-type natriuretic peptide). Elucidation of the 39-residue amino acid sequence confirms the homology with mammalian CNPs. These peptides produce hypotension in vivo and relax smooth muscle in vitro, but are poorly characterised in terms of physiological function. ovCNP-39 is equipotent with human/rat/porcine CNP-22 in eliciting cyclic guanosine 5'-monophosphate (cGMP) elevation in cultured vascular smooth muscle cells, suggesting that, like CNP, it acts through the ANP, natriuretic peptide receptor subtype. The direct elevation of cGMP in vascular smooth muscle by ovCNP-39 may underlie the vasodilatory effects of platypus envenomation. (C) 1998 Published by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:99 / 110
页数:12
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