三酰甘油和 1-O-酰基神经酰胺生物合成途径中酰基转移酶的药物靶向作用

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Maria Hernandez-Corbacho, Daniel Canals
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引用次数: 0

摘要

酰基转移酶(EC 2.3.)是一大类将酰基转移到多种底物上的酶。本综述重点介绍参与甘油酯和鞘脂生物合成途径的脂肪酰基转移酶,以及这些酶如何在其生物学背景下成为药理学靶标。甘油三酯和鞘磷脂在其调节和生物功能方面通常是独立处理的,本研究将它们放在一起,以强调其代谢和生物活性作用的平行性。此外,还讨论了一种新的信号分子--1-O-酰基甘油酰胺,它是由 DGAT2 酶酰化神经酰胺产生的。最后,探讨了 DGAT2 作为神经酰胺酰基转移酶(CAT)的意义,它在 TAG 和 1-O-acylceramide 生成中可能具有双重作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug targeting of acyltransferases in the Triacylglyceride and 1-O-AcylCeramide biosynthetic pathways
Acyltransferase enzymes (EC 2.3.) are a large group of enzymes that transfer acyl groups to a large variety of substrates. This review focuses on fatty acyltransferases involved in the biosynthetic pathways of glycerolipids and sphingolipids and how these enzymes have been pharmacologically targeted in their biological context. Glycerolipids and sphingolipids, commonly treated independently in their regulation and biological functions, are put together to emphasize the parallelism in their metabolism and bioactive roles. Furthermore, a newly considered signaling molecule, 1-O-acylceramide, resulting from the acylation of ceramide by DGAT2 enzyme, is discussed. Finally, the implications of DGAT2 as a putative Ceramide AcylTransferase (CAT) enzyme, with a putative dual role in TAG and 1-O-acylceramide generation, are explored.
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来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
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