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活性酪氨酸激酶结构域的重组表达方法:指南与陷阱

Methods for the recombinant expression of active tyrosine kinase domains: Guidelines and pitfalls.

作者信息

Díaz Galicia M Escarlet, Aldehaiman Abdullah, Hong SeungBeom, Arold Stefan T, Grünberg Raik

机构信息

Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.

Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.

出版信息

Methods Enzymol. 2019;621:131-152. doi: 10.1016/bs.mie.2019.02.027. Epub 2019 Mar 26.

Abstract

Protein tyrosine kinases (PTKs) are key signaling molecules and important drug targets. Although the efficient recombinant production of active PTKs is important for both pharmaceutical industry and academic research, most PTKs are still obtained from conventional, expensive and time-consuming insect-cell based expression. Host toxicity, kinase inactivity, insolubility and heterogeneity are among the reasons thought to preclude PTK expression in Escherichia coli. Herein we review these presumed roadblocks and their possible solutions for bacterial expression of PTKs, and give an overview on kinase activity assays. Finally, we report our experiences and observations with the kinases Src, Lyn and FAK as examples to illustrate implementation, effects and pitfalls of E. coli expression and in vitro assaying of PTKs.

摘要

蛋白质酪氨酸激酶(PTKs)是关键的信号分子和重要的药物靶点。尽管活性PTKs的高效重组生产对制药行业和学术研究都很重要,但大多数PTKs仍通过传统的、昂贵且耗时的基于昆虫细胞的表达来获得。宿主毒性、激酶无活性、不溶性和异质性被认为是阻碍PTKs在大肠杆菌中表达的部分原因。在此,我们综述这些假定的障碍及其解决PTKs在细菌中表达的可能方案,并概述激酶活性测定方法。最后,我们以激酶Src、Lyn和FAK为例报告我们的经验和观察结果,以说明大肠杆菌表达和PTKs体外测定的实施、效果及陷阱。

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