Bonfiglio Juan J, Colby Thomas, Matic Ivan
Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9b, Cologne 50931, Germany.
Nucleic Acids Res. 2017 Jun 20;45(11):6259-6264. doi: 10.1093/nar/gkx446.
Protein ADP-ribosylation (ADPr), a biologically and clinically important post-translational modification, exerts its functions by targeting a variety of different amino acids. Its repertoire recently expanded to include serine ADPr, which is emerging as an important and widespread signal in the DNA damage response. Chemically, serine ADPr (and more generally o-glycosidic ADPr) is a form of o-glycosylation, and its extreme lability renders it practically invisible to standard mass spectrometry approaches, often leading to erroneous localizations. The knowledge from the mature field of o-glycosation and our own initial difficulties with mass spectrometric analyzes of serine ADPr suggest how to avoid these misidentifications and fully explore the scope of o-glycosidic ADPr in DNA damage response and beyond.
蛋白质ADP-核糖基化(ADPr)是一种在生物学和临床上具有重要意义的翻译后修饰,它通过靶向多种不同的氨基酸来发挥其功能。其作用范围最近已扩展到包括丝氨酸ADPr,它正成为DNA损伤反应中一种重要且广泛存在的信号。从化学角度来看,丝氨酸ADPr(更普遍地说是O-糖苷键型ADPr)是O-糖基化的一种形式,其极高的不稳定性使得它在标准质谱方法中几乎无法被检测到,常常导致错误的定位。来自成熟的O-糖基化领域的知识以及我们自己在丝氨酸ADPr质谱分析中最初遇到的困难,提示了如何避免这些错误识别,并全面探索O-糖苷键型ADPr在DNA损伤反应及其他方面的作用范围。