Introducing protein deamidation: Landmark discoveries, societal outreach, and tentative priming workflow to address deamidation

被引:10
作者
Boudier-Lemosquet, Axel [1 ]
Mahler, Adrien [1 ]
Bobo, Claude [1 ]
Dufossée, Mélody [1 ]
Priault, Muriel [1 ]
机构
[1] Univ Bordeaux, CNRS, IBGC, UMR 5095, F-F33000 Bordeaux, France
关键词
Post-translational modification; Protein instability; Deamidation reaction mechanism; Deamidation historical milestones; Deamidation technical milestones; Artwork dating; Archaeology sample dating; Forensic analysis; CARBOXYL METHYLTRANSFERASE; NONENZYMATIC DEAMIDATION; ASPARAGINYL RESIDUES; L-ISOASPARTYL; TRIOSEPHOSPHATE ISOMERASE; GLUTAMINE DEAMIDATION; PEPTIDE DEGRADATION; ASPARTYL RESIDUES; CHEMICAL PATHWAYS; PRIMARY SEQUENCE;
D O I
10.1016/j.ymeth.2021.11.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Our current knowledge on protein deamidation results from a journey that started almost 100 years ago, when a handful of researchers first described the non-enzymatic "desamidation" of glutamine, and the effect of different anions on the catalytic rate of the reaction. Since then, the field has tremendously expended and now finds outreach in very diverse areas. In light of all the recent articles published in these areas, it seemed timely to propose an integrated review on the subject, including a short historical overview of the landmark discoveries in the field, highlighting the current global positioning of protein deamidation in biology and non-biology fields, and concluding with a workflow for those asking if a protein can deamidate, and identify the residues involved. This review is essentially intended to provide newcomers in the field with an overview of how deamidation has penetrated our society and what tools are currently at hand to identify and quantify protein deamidation.
引用
收藏
页码:3 / 14
页数:12
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