Institutes for Advanced Interdisciplinary Research, East China Normal University, 3663 N. Zhongshan Road, Shanghai 200062, China.
J Pept Sci. 2013 Sep;19(9):598-605. doi: 10.1002/psc.2538. Epub 2013 Jul 26.
Glucagon-like peptide 1 receptor (GLP1R) is a promising target for the treatment of type 2 diabetes. Because of the short half-life of endogenous GLP1 peptide, other GLP1R agonists are considered to be appealing therapeutic candidates. A high-throughput assay has been established to screen for GLP1R agonists in a 60 000-well natural product compound library fractionated from 670 different herbs/materials widely used in traditional Chinese medicines (TCMs). The screening is based on primary screen of GLP1R⁺ reporter gene assay with the counter screen in GLP1R⁻ cell line. An active fraction, A089-147, was identified from the screening. Fraction A089-147 was isolated from dried Ophisaurus harti, and the fact that its GLP1R agonist activity was sensitive to trypsin treatment indicates its peptidic nature. The active ingredient of A089-147 was later identified as O. harti GLP1 through transcriptome analysis. Chemically synthesized O. harti GLP1 showed GLP1R agonist activity and sensitivity to dipeptidase IV digestion. This study illustrated a comprehensive screening strategy to identify novel GLP1R agonists from TCMs libraries and at the same time underlined the difficulty of identifying a non-peptidic GLP1R agonist. The novel O. harti GLP1 peptide yielded from this study confirmed broader application of TCMs libraries in active peptide identification.
胰高血糖素样肽 1 受体 (GLP1R) 是治疗 2 型糖尿病的有前途的靶点。由于内源性 GLP1 肽的半衰期短,其他 GLP1R 激动剂被认为是有吸引力的治疗候选物。已经建立了高通量测定法,以从广泛用于中药的 670 种不同草药/材料的 60,000 孔天然产物化合物库中筛选 GLP1R 激动剂。筛选基于 GLP1R⁺报告基因测定的初步筛选,并用 GLP1R⁻细胞系进行反筛。从筛选中鉴定出一个活性部分 A089-147。A089-147 部分从干燥的蛇晰中分离得到,其 GLP1R 激动剂活性对胰蛋白酶处理敏感表明其具有肽性质。A089-147 的活性成分后来通过转录组分析被鉴定为 O. harti GLP1。化学合成的 O. harti GLP1 表现出 GLP1R 激动剂活性和对二肽酶 IV 消化的敏感性。本研究说明了一种全面的筛选策略,可从中药库中鉴定新型 GLP1R 激动剂,同时强调了鉴定非肽 GLP1R 激动剂的困难。从这项研究中获得的新型 O. harti GLP1 肽证实了中药库在活性肽鉴定方面的更广泛应用。