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蛋白酪氨酸磷酸酶 1B 抑制剂依替膦酸二钠的作用模式。

The mode of action of the Protein tyrosine phosphatase 1B inhibitor Ertiprotafib.

机构信息

Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona, United States of America.

出版信息

PLoS One. 2020 Oct 2;15(10):e0240044. doi: 10.1371/journal.pone.0240044. eCollection 2020.

Abstract

Protein tyrosine phosphatase 1B (PTP1B) is a validated therapeutic target for the treatment of diabetes and obesity. Ertiprotafib is a PTP1B inhibitor that reached the clinical trial stage for the treatment of diabetes. Interestingly, Ertiprotafib reduces the melting temperature of PTP1B in differential scanning fluorimetry (DSF) assays, different from most drugs that increase the stability of their target upon binding. No molecular data on how Ertiprotafib functions has been published. Thus, to gain molecular insights into the mode of action of Ertiprotafib, we used biomolecular NMR spectroscopy to characterize the molecular details of the PTP1B:Ertiprotafib interaction. Our results show that Ertiprotafib induces aggregation of PTP1B in a concentration dependent manner. This shows that the insufficient clinical efficacy and adverse effects caused by Ertiprotafib is due to its tendency to cause aggregation of PTP1B.

摘要

蛋白酪氨酸磷酸酶 1B(PTP1B)是治疗糖尿病和肥胖症的有效治疗靶点。Ertiprotafib 是一种 PTP1B 抑制剂,已进入治疗糖尿病的临床试验阶段。有趣的是,Ertiprotafib 在差示扫描荧光法(DSF)测定中降低了 PTP1B 的熔点,与大多数增加其靶标结合稳定性的药物不同。目前尚未发表关于 Ertiprotafib 如何发挥作用的分子数据。因此,为了深入了解 Ertiprotafib 的作用机制,我们使用生物分子 NMR 光谱学来表征 PTP1B:Ertiprotafib 相互作用的分子细节。我们的结果表明,Ertiprotafib 以浓度依赖的方式诱导 PTP1B 聚集。这表明 Ertiprotafib 导致的临床疗效不足和不良反应是由于其引起 PTP1B 聚集的倾向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b7/7531832/934566150a07/pone.0240044.g001.jpg

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