Helokinestatin-7 peptides from the venoms of Heloderma lizards

Chengbang Ma, Hui Wang, Yuxin Wu, Mei Zhou, Gemma Lowe, Lei Wang, Yingqi Zhang, Tianbao Chen, Christopher Shaw

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Helokinestatins 1–6 constitute a family of bradykinin antagonist peptides originally isolated from the venoms of the Gila Monster, Heloderma suspectum and the Mexican beaded lizard, Heloderma horridum. Here we report the identification, isolation and preliminary pharmacological characterization of two novel tridecapeptides, named helokinestatin-7S (FDDDSTELILEPR – 1550 Da) and helokinestatin-7H (FDDDSRKLILEPR – 1604 Da), whose primary structures were predicted from cDNAs cloned from venom libraries of respective Heloderma lizards. Computed molecular masses of putative helokinestatin-7 peptides were used as tools to locate these peptides in archived LC/MS fractions from respective venoms and sequences were confirmed by MS/MS fragmentation. A synthetic replicate of helokinestatin-7H was found to antagonize the relaxation effect of bradykinin on rat arterial smooth muscle but to have no measurable effects alone. In contrast, synthetic helokinestatin-7S was found to directly contract this preparation. Studies on related natural peptides with subtle differences in primary structure can provide the tools for structure/activity studies in pharmacological investigations directed toward unraveling the molecular basis of venom toxicity and for the evaluation of potential therapeutic leads.Highlights

► The paper describes two novel peptides, helokinestatin-7S and helokinestatin-7H. ► Helokinestatin-7S is from the venom of the Gila Monster (Heloderma suspectum). ► Helokinestatin-7H is from the venom of the Mexican beaded lizard (Heloderma horridum). ► Helokinestatin-7 peptides had different effects on rat tail artery smooth muscle.

Original languageEnglish
Pages (from-to)300-305
Number of pages6
JournalPeptides
Volume35
Issue number2
Early online date05 Apr 2012
DOIs
Publication statusPublished - Jun 2012
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology
  • Physiology
  • Cellular and Molecular Neuroscience

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