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N 端靶向蛋白质修饰化学的选择性和稳定性。

Selectivity and stability of N-terminal targeting protein modification chemistries.

作者信息

Barber Lydia J, Yates Nicholas D J, Fascione Martin A, Parkin Alison, Hemsworth Glyn R, Genever Paul G, Spicer Christopher D

机构信息

Department of Chemistry, University of York Heslington YO10 5DD UK

York Biomedical Research Institute, University of York Heslington YO10 5DD UK.

出版信息

RSC Chem Biol. 2022 Nov 17;4(1):56-64. doi: 10.1039/d2cb00203e. eCollection 2023 Jan 4.

Abstract

Protein N-termini provide uniquely reactive motifs for single site protein modification. Though a number of reactions have been developed to target this site, the selectivity, generality, and stability of the conjugates formed has not been studied. We have therefore undertaken a comprehensive comparative study of the most promising methods for N-terminal protein modification, and find that there is no 'one size fits all' approach, necessitating reagent screening for a particular protein or application. Moreover, we observed limited stability in all cases, leading to a need for continued innovation and development in the bioconjugation field.

摘要

蛋白质N端为单一位点蛋白质修饰提供了独特的反应基序。尽管已经开发了许多靶向该位点的反应,但所形成缀合物的选择性、通用性和稳定性尚未得到研究。因此,我们对最有前景的N端蛋白质修饰方法进行了全面的比较研究,发现不存在“一刀切”的方法,需要针对特定蛋白质或应用进行试剂筛选。此外,我们观察到在所有情况下稳定性都有限,这导致生物缀合领域需要持续创新和发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ef/9811658/b6b270b24274/d2cb00203e-f1.jpg

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