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酰化偶联亲脂性极化诱导法(Acyl-cLIP):一种用于脂质转移酶和水解酶的通用检测方法。

Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes.

作者信息

Lanyon-Hogg Thomas, Ritzefeld Markus, Sefer Lea, Bickel Jasmine K, Rudolf Amalie F, Panyain Nattawadee, Bineva-Todd Ganka, Ocasio Cory A, O'Reilly Nicola, Siebold Christian, Magee Anthony I, Tate Edward W

机构信息

Department of Chemistry , Imperial College London , London , W12 0BZ , UK . Email:

Division of Structural Biology , Wellcome Centre for Human Genetics , University of Oxford , Oxford , OX3 7BN , UK.

出版信息

Chem Sci. 2019 Jul 1;10(39):8995-9000. doi: 10.1039/c9sc01785b. eCollection 2019 Oct 21.

Abstract

Posttranslational attachment of lipids to proteins is important for many cellular functions, and the enzymes responsible for these modifications are implicated in many diseases, from cancer to neurodegeneration. Lipid transferases and hydrolases are increasingly tractable therapeutic targets, but present unique challenges for high-throughput biochemical enzyme assays which hinder development of new inhibitors. We present Acylation-coupled Lipophilic Induction of Polarisation (Acyl-cLIP) as the first universally applicable biochemical lipidation assay, exploiting the hydrophobic nature of lipidated peptides to drive a polarised fluorescence readout. Acyl-cLIP allows sensitive, accurate, real-time measurement of - or -palmitoylation, -myristoylation, -farnesylation or -geranylgeranylation. Furthermore, it is applicable to transfer and hydrolysis reactions, and we demonstrate its extension to a high-throughput screening format. We anticipate that Acyl-cLIP will greatly expedite future drug discovery efforts against these challenging targets.

摘要

蛋白质的翻译后脂质修饰对于许多细胞功能至关重要,负责这些修饰的酶与从癌症到神经退行性疾病等多种疾病有关。脂质转移酶和水解酶越来越成为易于处理的治疗靶点,但对于高通量生化酶分析而言存在独特挑战,这阻碍了新型抑制剂的开发。我们提出了酰化偶联亲脂性极化诱导法(Acyl-cLIP),这是首个普遍适用的生化脂化分析方法,利用脂化肽的疏水性质来驱动极化荧光读数。Acyl-cLIP能够灵敏、准确、实时地测量α-或ω-棕榈酰化、N-肉豆蔻酰化、法尼基化或香叶基香叶基化。此外,它适用于转移和水解反应,我们还展示了其向高通量筛选形式的扩展。我们预计Acyl-cLIP将极大地加快未来针对这些具有挑战性靶点的药物发现工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4859/6855259/24fde6a07a7c/c9sc01785b-f1.jpg

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