Demyanenko Yana, Sui Xintong, Giltrap Andrew M, Davis Benjamin G, Kuster Bernhard, Mohammed Shabaz
The Rosalind Franklin Institute, Harwell, UK; Department of Pharmacology, University of Oxford, Oxford, UK.
Chair of Proteomics and Bioanalytics, Technical University of Munich, Freising, Germany.
Mol Cell Proteomics. 2025 Apr;24(4):100948. doi: 10.1016/j.mcpro.2025.100948. Epub 2025 Mar 13.
N-hydroxysuccinimide (NHS) ester chemistry is used extensively across proteomics sample preparation. One of its increasingly prevalent applications is in isobaric reagent-based quantitation such as isobaric tags for relative and absolute quantitation and tandem mass tag approaches. In these methods, labeling on the primary amines of lysine residues and N termini of tryptic peptides via amide formation (N-derivatives) from corresponding NHS ester reagents is the intended reactive outcome. However, the role of NHS esters as activated carboxyls can also drive the formation of serine-, tyrosine-, and threonine-derived esters (O-derivatives). These O-derivative peptides are typically classed as overlabeled and are disregarded for quantitation, leading to loss of information and hence potential sensitivity. Their presence also unnecessarily increases sample complexity, which reduces the overall identification rates. One common approach for removing these unwanted labeling events has involved treatment with hydroxylamine. We show here that this approach is not efficient and can still leave substantial levels of unwanted overlabeled peptides. Through systematic study of nucleophilic aminolysis reagents and reaction conditions, we have now developed a robust method to efficiently remove overlabeled peptides. The new method reduces the proportion of overlabeled peptides in the sample to less than 1% without affecting the labeling rate or introducing other modifications, leading to superior identification rates and quantitation precision.
N-羟基琥珀酰亚胺(NHS)酯化学在蛋白质组学样品制备中被广泛应用。其越来越普遍的应用之一是在基于等压试剂的定量分析中,如相对和绝对定量的等压标签法以及串联质谱标签法。在这些方法中,通过相应的NHS酯试剂经酰胺形成(N-衍生物)对赖氨酸残基的伯胺和胰蛋白酶肽的N端进行标记是预期的反应结果。然而,NHS酯作为活化羧基的作用也会促使丝氨酸、酪氨酸和苏氨酸衍生酯(O-衍生物)的形成。这些O-衍生物肽通常被归类为过度标记,在定量分析时被忽略,导致信息丢失,从而降低了潜在的灵敏度。它们的存在还不必要地增加了样品复杂性,进而降低了整体鉴定率。一种去除这些不必要标记事件的常见方法是用羟胺处理。我们在此表明,这种方法效率不高,仍然会留下大量不需要的过度标记肽。通过对亲核氨解试剂和反应条件的系统研究,我们现在开发了一种有效的方法来高效去除过度标记的肽。新方法将样品中过度标记肽的比例降低到1%以下,而不影响标记率或引入其他修饰,从而实现了更高的鉴定率和定量精度。