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动态蛋白质酰化:新的底物、机制和药物靶点。

Dynamic Protein Acylation: New Substrates, Mechanisms, and Drug Targets.

机构信息

Institute of Chemical Biology, Department of Chemistry, Imperial College London, London SW7 2AZ, UK.

Institute of Chemical Biology, Department of Chemistry, Imperial College London, London SW7 2AZ, UK.

出版信息

Trends Biochem Sci. 2017 Jul;42(7):566-581. doi: 10.1016/j.tibs.2017.04.004. Epub 2017 Jun 8.

Abstract

Post-translational attachment of lipids to proteins is found in all organisms, and is important for many biological processes. Acylation with myristic and palmitic acids are among the most common lipid modifications, and understanding reversible protein palmitoylation dynamics has become a particularly important goal. Linking acyltransferase enzymes to disease states can be challenging due to a paucity of robust models, compounded by functional redundancy between many palmitoyl transferases; however, in cases such as Wnt or Hedgehog signalling, small molecule inhibitors have been identified, with some progressing to clinical trials. In this review, we present recent developments in our understanding of protein acylation in human health and disease through use of chemical tools, global profiling of acylated proteomes, and functional studies of specific protein targets.

摘要

蛋白质的翻译后脂质附着存在于所有生物体中,对许多生物过程都很重要。与豆蔻酸和棕榈酸的酰化是最常见的脂质修饰之一,理解可逆的蛋白质棕榈酰化动力学已成为一个特别重要的目标。由于缺乏稳健的模型,许多棕榈酰转移酶之间存在功能冗余,将酰基转移酶酶与疾病状态联系起来具有挑战性;然而,在 Wnt 或 Hedgehog 信号等情况下,已经确定了小分子抑制剂,其中一些已进入临床试验。在这篇综述中,我们通过使用化学工具、酰化蛋白质组的全局分析以及特定蛋白质靶标的功能研究,介绍了我们在人类健康和疾病中对蛋白质酰化理解的最新进展。

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