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通过遗传密码扩展研究乌头酸酶同工酶的乙酰化作用。

Studying Acetylation of Aconitase Isozymes by Genetic Code Expansion.

作者信息

Araujo Jessica, Ottinger Sara, Venkat Sumana, Gan Qinglei, Fan Chenguang

机构信息

Cell and Molecular Biology Program, University of Arkansas, Fayetteville, AR, United States.

Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR, United States.

出版信息

Front Chem. 2022 Mar 24;10:862483. doi: 10.3389/fchem.2022.862483. eCollection 2022.

Abstract

Aconitase catalyzes the second reaction of the tricarboxylic acid cycle, the reversible conversion of citrate and isocitrate. has two isoforms of aconitase, AcnA and AcnB. Acetylomic studies have identified acetylation at multiple lysine sites of both aconitase isozymes, but the impacts of acetylation on aconitases are unknown. In this study, we applied the genetic code expansion approach to produce 14 site-specifically acetylated aconitase variants. Enzyme assays and kinetic analyses showed that acetylation of AcnA K684 decreased the enzyme activity, while acetylation of AcnB K567 increased the enzyme activity. Further acetylation and deacetylation assays were performed, which indicated that both aconitase isozymes could be acetylated by acetyl-phosphate chemically, and be deacetylated by the CobB deacetylase at most lysine sites. Through this study, we have demonstrated practical applications of genetic code expansion in acetylation studies.

摘要

乌头酸酶催化三羧酸循环的第二步反应,即柠檬酸和异柠檬酸的可逆转化。乌头酸酶有两种同工型,AcnA和AcnB。乙酰化蛋白质组学研究已确定这两种乌头酸酶同工型的多个赖氨酸位点发生了乙酰化,但乙酰化对乌头酸酶的影响尚不清楚。在本研究中,我们应用遗传密码扩展方法制备了14种位点特异性乙酰化的乌头酸酶变体。酶活性测定和动力学分析表明,AcnA K684位点的乙酰化降低了酶活性,而AcnB K567位点的乙酰化增加了酶活性。进一步进行了乙酰化和去乙酰化试验,结果表明,两种乌头酸酶同工型均可被乙酰磷酸化学乙酰化,并在大多数赖氨酸位点被CobB去乙酰化酶去乙酰化。通过本研究,我们展示了遗传密码扩展在乙酰化研究中的实际应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/274e/8987015/7aadf32ee6b1/fchem-10-862483-g001.jpg

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