Thilini Abeywansha, Abigail Kim, Sahil Bhaskaran, Yi Zhang
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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).
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.