肽
染色质
化学
体内
兴奋剂
内分泌学
内科学
受体
生物化学
生物
医学
生物技术
渔业
作者
Liqian Gao,Zhiqiang Yu,Meng Dan,Fang Zheng,Yong Ong,Peng Miao,Su Seong Lee,Longping Wen
出处
期刊:Protein and Peptide Letters
[Bentham Science]
日期:2015-07-13
卷期号:22 (8): 762-766
被引量:13
标识
DOI:10.2174/0929866522666150622101944
摘要
An α-MSH peptide analogue, named MTII (Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]- NH2), is one of the most important ligands of melanotropic receptors but are relatively nonselective. In order to improve the melanotropic activities of the well-characterized MTII analogues, we report here a new analogue by modifying the core structure as well as the size of the cyclic region of MTII peptide. The analogue peptide, Ac-Nle-c[Asp-His-D-Phe-Lys-Trp-Gly-Lys]-OH (F Peptide), in which we replaced Arg at position 8 with Lys and added a Gly to position 10 of the MTII peptide sequence, was synthesized and used as a new melanotropic hormone in controlling rapid color changes in frogs by its actions on mobilizing pigment granule movements within chromatophores. The in vivo responses of chromatophores to MTII and the related analogue F Peptide were studied in frogs. The results show that the F Peptide was a superpotent agonist with similar melanotropic activity to the MTII peptide according to MTII peptide by in vivo studies. The analogue also exhibited ultraprolonged melanotropic activity. The F peptide can be useful in the study of numerous physiological processes, particularly when superpotent and prolonged melanotropic activity is desired. Keywords: Antagonist, F peptide, frog skin, Melanophore Index, melanotropic activity, MTII peptide.
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