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人ATE1精氨酰转移酶的重组表达、纯化及特性分析

Recombinant expression, purification, and characterization of human ATE1 arginyltransferase.

作者信息

Abeywansha Thilini, Kim Abigail, Bhaskaran Sahil, Zhang Yi

机构信息

Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH, United States.

Department of Biology, Case Western Reserve University, Cleveland, OH, United States.

出版信息

Methods Enzymol. 2025;718:283-294. doi: 10.1016/bs.mie.2025.06.020. Epub 2025 Jul 5.

Abstract

This chapter presents a straightforward method for expressing and purifying recombinant human Arginyl-tRNA-protein transferase 1 (ATE1) from E. coli. ATE1 is an enzyme that catalyzes the transfer of arginine from arginyl-tRNA to the N-terminal or internal Asp or Glu residues of the substrate proteins, a process that regulates protein turnover or function. The approach enables the efficient purification of milligram-scale quantities of highly soluble, enzymatically active ATE1 with over 98 % purity. Additionally, we describe the procedures for validating human ATE1 activity through an arginylation assay followed by mass spectrometry. We also describe the quantification of ATE1-tRNA binding affinity using Electrophoretic Mobility Shift Assay (EMSA).

摘要

本章介绍了一种从大肠杆菌中表达和纯化重组人精氨酰 - tRNA - 蛋白质转移酶1(ATE1)的直接方法。ATE1是一种催化精氨酸从精氨酰 - tRNA转移到底物蛋白质的N端或内部天冬氨酸或谷氨酸残基上的酶,这一过程调节蛋白质的周转或功能。该方法能够高效纯化毫克级数量的高溶解性、具有酶活性且纯度超过98%的ATE1。此外,我们描述了通过精氨酰化测定随后进行质谱分析来验证人ATE1活性的程序。我们还描述了使用电泳迁移率变动分析(EMSA)对ATE1 - tRNA结合亲和力进行定量的方法。

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