人ATE1精氨酸转移酶的重组表达、纯化和特性研究。

4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology
Methods in enzymology Pub Date : 2025-01-01 Epub Date: 2025-07-05 DOI:10.1016/bs.mie.2025.06.020
Thilini Abeywansha, Abigail Kim, Sahil Bhaskaran, Yi Zhang
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引用次数: 0

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酸- trna -蛋白转移酶1 (ATE1)的简单方法。ATE1是一种催化精氨酸从精氨酸- trna转移到底物蛋白的n端或内部Asp或Glu残基的酶,这一过程调节蛋白质的周转或功能。该方法可以高效纯化毫克级的高可溶性、酶活性ATE1,纯度超过98%。此外,我们描述了通过精氨酸化分析和质谱分析验证人类ATE1活性的程序。我们还描述了使用电泳迁移转移法(EMSA)定量ATE1-tRNA结合亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recombinant expression, purification, and characterization of human ATE1 arginyltransferase.

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).

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来源期刊
Methods in enzymology
Methods in enzymology 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
308
审稿时长
3-6 weeks
期刊介绍: The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.
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