Identification of Miscellaneous Peptides from the Skin Secretion of the European Edible Frog, Pelophylax kl. Esculentus

被引:0
作者
Xiaole Chen
He Wang
Lei Wang
Mei Zhou
Tianbao Chen
Chris Shaw
机构
[1] Fujian Medical University,School of Pharmacy
[2] Fujian University of Traditional Chinese Medicine,School of Integrative Medicine
[3] Queen’s University,Medicine Natural Peptide Discovery Group, School of Pharmacy
来源
The Protein Journal | 2016年 / 35卷
关键词
Amphibian; Secretion; Mass spectrometry; Peptide; Cloning;
D O I
暂无
中图分类号
学科分类号
摘要
The chemical compounds synthesised and secreted from the dermal glands of amphibian have diverse bioactivities that play key roles in the hosts’ innate immune system and in causing diverse pharmacological effects in predators that may ingest the defensive skin secretions. As new biotechnological methods have developed, increasing numbers of novel peptides with novel activities have been discovered from this source of natural compounds. In this study, a number of defensive skin secretion peptide sequences were obtained from the European edible frog, P. kl. esculentus, using a ‘shotgun’ cloning technique developed previously within our laboratory. Some of these sequences have been previously reported but had either obtained from other species or were isolated using different methods. Two new skin peptides are described here for the first time. Esculentin-2c and Brevinin-2Tbe belong to the Esculentin-2 and Brevinin-2 families, respectively, and both are very similar to their respective analogues but with a few amino acid differences. Further, [Asn-3, Lys-6, Phe-13] 3-14-bombesin isolated previously from the skin of the marsh frog, Rana ridibunda, was identified here in the skin of P. kl. esculentus. Studies such as this can provide a rapid elucidation of peptide and corresponding DNA sequences from unstudied species of frogs and can rapidly provide a basis for related scientific studies such as those involved in systematic or the evolution of a large diverse gene family and usage by biomedical researchers as a source of potential novel drug leads or pharmacological agents.
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页码:291 / 299
页数:8
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