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通过肽诱变开发新型胰淀素和降钙素受体激活剂。

Development of the novel amylin and calcitonin receptor activators by peptide mutagenesis.

作者信息

Lee Sangmin

机构信息

Department of Medicinal Biotechnology, College of Health Science, Dong-A University, Busan, 49315, Republic of Korea.

出版信息

Arch Biochem Biophys. 2024 Dec;762:110191. doi: 10.1016/j.abb.2024.110191. Epub 2024 Oct 29.

DOI:10.1016/j.abb.2024.110191
PMID:39481742
Abstract

The amylin peptide hormone receptor is the complex of the calcitonin peptide hormone receptor and an accessory protein. The calcitonin receptor activation controls calcium homeostasis, while it also functions as the main component of the amylin receptor. Amylin receptor activation in brains controls blood glucose and appetite. Currently, non-selective amylin and calcitonin receptor activators have been tested for body weight reduction to treat obesity. Here, multiple peptide activators for human amylin and calcitonin receptors were developed by introducing comprehensive mutagenesis to rat amylin peptide. The rat amylin peptide C-terminal fragment that interacts with amylin receptor extracellular domain was used to screen for affinity-enhancing mutations. Up to twelve mutational combinations were found to significantly increase peptide affinity both for amylin and calcitonin receptor extracellular domains by over 100-fold. Using these affinity-enhancing mutations, three representative rat amylin analogs with thirty-seven amino acids were made to test the potency increase for amylin and calcitonin receptor activation. All three mutated rat amylin analogs showed significant potency increases by 5- to 10-fold compared to endogenous rat amylin. These mutated peptide activators also showed higher potency for human amylin and calcitonin receptor activation than a clinically available amylin receptor activator pramlintide. These amylin and calcitonin receptor activators developed in this study may be useful as the valuable pharmacological tools that activate amylin receptors in cell-based systems.

摘要

胰淀素肽激素受体是降钙素肽激素受体与一种辅助蛋白的复合物。降钙素受体激活可控制钙稳态,同时它也是胰淀素受体的主要组成部分。大脑中胰淀素受体的激活可控制血糖和食欲。目前,非选择性的胰淀素和降钙素受体激活剂已被用于测试减轻体重以治疗肥胖症。在此,通过对大鼠胰淀素肽进行全面诱变,开发了多种针对人胰淀素和降钙素受体的肽激活剂。利用与胰淀素受体细胞外结构域相互作用的大鼠胰淀素肽C末端片段来筛选亲和力增强突变。发现多达十二种突变组合可使肽对胰淀素和降钙素受体细胞外结构域的亲和力显著增加超过100倍。利用这些亲和力增强突变,制备了三种具有37个氨基酸的代表性大鼠胰淀素类似物,以测试胰淀素和降钙素受体激活的效力增加情况。与内源性大鼠胰淀素相比,所有三种突变的大鼠胰淀素类似物的效力均显著增加了5至10倍。这些突变的肽激活剂对人胰淀素和降钙素受体激活的效力也高于临床上可用的胰淀素受体激活剂普兰林肽。本研究中开发的这些胰淀素和降钙素受体激活剂可能作为在基于细胞的系统中激活胰淀素受体的有价值的药理学工具。

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