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利用重组 SnRK2 进行体外激酶分析:用于测定植物中应激响应激酶的示例。

In Vitro Kinase Assay with Recombinant SnRK2s: An Example for Assaying Stress-Responsive Kinases in Plants.

机构信息

Department of Life Technologies, University of Turku, Turku, Finland.

出版信息

Methods Mol Biol. 2024;2832:163-170. doi: 10.1007/978-1-0716-3973-3_11.

Abstract

Protein phosphorylation is one of the most important posttranslational modifications in cell signaling pathways. Kinases and phosphatases play essential roles in transferring information between sensors and effectors under stress conditions. Several methods have been developed to analyze the phosphorylation mechanisms. Each method has advantages and disadvantages. In vitro kinase assay using recombinant proteins is a method to analyze kinase activities under simplified conditions. It is a good strategy to understand each mechanism one by one, although it is not always suitable to estimate the feature of complex machinery in vivo. In this chapter, the purification of recombinant proteins produced in Escherichia coli followed by assaying a kinase activity using radioactivity is described.

摘要

蛋白质磷酸化是细胞信号通路中最重要的翻译后修饰之一。激酶和磷酸酶在应激条件下传感器和效应器之间的信息传递中发挥着重要作用。已经开发了几种方法来分析磷酸化机制。每种方法都有其优点和缺点。使用重组蛋白的体外激酶测定是在简化条件下分析激酶活性的一种方法。虽然它并不总是适用于估计体内复杂机制的特征,但逐个了解每个机制是一种很好的策略。在本章中,描述了使用放射性物质测定激酶活性的大肠杆菌中重组蛋白的纯化。

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