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鞣花酸及其代谢物作为肝丙酮酸激酶的有效和选择性别构抑制剂。

Ellagic Acid and Its Metabolites as Potent and Selective Allosteric Inhibitors of Liver Pyruvate Kinase.

机构信息

Department of Chemistry and Molecular Biology, University of Gothenburg, 412 96 Gothenburg, Sweden.

Science for Life Laboratory, KTH-Royal Institute of Technology, 104 50 Stockholm, Sweden.

出版信息

Nutrients. 2023 Jan 22;15(3):577. doi: 10.3390/nu15030577.

Abstract

Liver pyruvate kinase (PKL) has recently emerged as a new target for non-alcoholic fatty liver disease (NAFLD), and inhibitors of this enzyme could represent a new therapeutic option. However, this breakthrough is complicated by selectivity issues since pyruvate kinase exists in four different isoforms. In this work, we report that ellagic acid (EA) and its derivatives, present in numerous fruits and vegetables, can inhibit PKL potently and selectively. Several polyphenolic analogues of EA were synthesized and tested to identify the chemical features responsible for the desired activity. Molecular modelling studies suggested that this inhibition is related to the stabilization of the PKL inactive state. This unique inhibition mechanism could potentially herald the development of new therapeutics for NAFLD.

摘要

肝丙酮酸激酶(PKL)最近成为非酒精性脂肪性肝病(NAFLD)的一个新靶点,这种酶的抑制剂可能代表一种新的治疗选择。然而,由于丙酮酸激酶存在于四种不同的同工酶中,因此选择性问题使这一突破变得复杂。在这项工作中,我们报告了鞣花酸(EA)及其衍生物(存在于许多水果和蔬菜中)能够有效地选择性抑制 PKL。合成了几种 EA 的多酚类类似物,并进行了测试以确定导致所需活性的化学特征。分子建模研究表明,这种抑制与 PKL 无活性状态的稳定有关。这种独特的抑制机制可能为 NAFLD 的新疗法的开发提供契机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/683f/9919951/01707be2ec08/nutrients-15-00577-sch002.jpg

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