Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského 1203/8, 500 05 Hradec Králové, Czech Republic.
J Proteome Res. 2020 Mar 6;19(3):993-999. doi: 10.1021/acs.jproteome.9b00823. Epub 2020 Feb 20.
The ability of concentrated formic acid to formylate reactive amino acid residues is known from previous reports. In contrast, solvents containing a low concentration of formic acid are generally recognized as a safe environment for proteomic applications. The primary objective of this study was to explain the excessive formylation rate in tryptic peptides that did not come into contact with concentrated formic acid. We found out that the peptide formylation was associated with dissolving the peptides in a solvent containing mere 0.1% formic acid. Similar conclusions were drawn after analyzing publicly available proteomic data. We further demonstrated that these unwanted modifications can be averted via handling the samples at a low temperature or, obviously, via replacing formic acid in the solvent with trifluoroacetic acid. These simple countermeasures can contribute to a reduction in the part of the MS/MS spectra that remain unassigned to a peptide sequence.
浓甲酸使反应性氨基酸残基甲酰化的能力在前人的报道中已有记载。相比之下,含低浓度甲酸的溶剂通常被认为是蛋白质组学应用的安全环境。本研究的主要目的是解释与未接触浓甲酸的胰蛋白酶肽的过度甲酰化率。我们发现,肽甲酰化与在仅含 0.1%甲酸的溶剂中溶解肽有关。在分析公开的蛋白质组学数据后得出了类似的结论。我们进一步证明,通过在低温下处理样品,或者通过用三氟乙酸代替溶剂中的甲酸,可以避免这些不需要的修饰。这些简单的对策可以减少未分配给肽序列的 MS/MS 谱部分。