Okyem Samuel, Sweedler Jonathan V
Department of Chemistry, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Mass Spectrom Rev. 2024 Nov 18. doi: 10.1002/mas.21916.
One of the great triumphs of mass spectrometry-based peptide and protein characterization is the characterization of their modifications as most modifications have a characteristic mass shift. What happens when the modification does not change the mass of the peptide? Here, the characterization of several peptide and proteins modifications that do not involve a mass shift are highlighted. Protein and peptide synthesis on ribosomes involves L-amino acids; however, posttranslational modifications (PTMs) can convert these L-amino acids into their D-isomers. As another example, nonenzymatic PTM of aspartate leads to the formation of three different isomers, with isoaspartate being the most prevalent. Both modifications do not alter the mass of the peptide and yet can have profound impact on the physicochemical characteristics of the peptide. Several MS and ion mobility techniques are highlighted, as are other methods such as chromatography, enzymatic enrichment, and labeling. The challenges inherent to these analytical methods and prospective developments in bioinformatics and computational strategies are discussed for these zero-dalton PTMs.
基于质谱的肽和蛋白质表征的重大成就之一是对其修饰进行表征,因为大多数修饰都有特征性的质量位移。当修饰不改变肽的质量时会发生什么?本文重点介绍了几种不涉及质量位移的肽和蛋白质修饰的表征。核糖体上的蛋白质和肽合成涉及L-氨基酸;然而,翻译后修饰(PTM)可将这些L-氨基酸转化为其D-异构体。再举一个例子,天冬氨酸的非酶促PTM会导致形成三种不同的异构体,其中异天冬氨酸最为普遍。这两种修饰都不会改变肽的质量,但却会对肽的物理化学特性产生深远影响。本文重点介绍了几种质谱和离子淌度技术,以及其他方法,如色谱法、酶富集法和标记法。针对这些零道尔顿PTM,讨论了这些分析方法固有的挑战以及生物信息学和计算策略的未来发展。