Mass Spectrometry Laboratory, GIGA-Research, University of Liege, Allee de la Chimie, 3, BAT B6c, 4000, Liege, Belgium.
J Am Soc Mass Spectrom. 2012 Mar;23(3):469-74. doi: 10.1007/s13361-011-0307-5. Epub 2011 Dec 20.
One of the mechanisms leading to MALDI in-source decay (MALDI ISD) is the transfer of hydrogen radicals to analytes upon laser irradiation. Analytes such as peptides or proteins may undergo ISD and this method can therefore be exploited for top-down sequencing. When performed on peptides, radical-induced ISD results in production of c- and z-ions, as also found in ETD and ECD activation. Here, we describe two new compounds which, when used as MALDI matrices, are able to efficiently induce ISD of peptides and proteins: 2-aminobenzamide and 2-aminobenzoic acid. In-source reduction of the disulfide bridge containing peptide Calcitonin further confirmed the radicalar mechanism of the ISD process. ISD of peptides led, in addition to c- and z-ions, to the generation of a-, x-, and y-ions both in positive and in negative ion modes. Finally, good sequence coverage was obtained for the sequencing of myoglobin (17 kDa protein), confirming the effectiveness of both 2-aminobenzamide and 2-aminobenzoic acid as MALDI ISD matrices.
导致基质辅助激光解吸电离(MALDI)源内降解(MALDI ISD)的机制之一是激光照射时氢自由基向分析物的转移。 肽或蛋白质等分析物可能会经历 ISD,因此可以利用这种方法进行自上而下的测序。 在对肽进行分析时,自由基诱导的 ISD 导致 c-和 z-离子的产生,这也在 ETD 和 ECD 激活中发现。 在这里,我们描述了两种新的化合物,当用作 MALDI 基质时,它们能够有效地诱导肽和蛋白质的 ISD:2-氨基苯甲酰胺和 2-氨基苯甲酸。 含有二硫键的肽降钙素的源内还原进一步证实了 ISD 过程的自由基机制。 除了 c-和 z-离子外,肽的 ISD 还导致正离子和负离子模式下的 a-、x-和 y-离子的生成。 最后,通过对肌红蛋白(17 kDa 蛋白)的测序获得了良好的序列覆盖率,证实了 2-氨基苯甲酰胺和 2-氨基苯甲酸作为 MALDI ISD 基质的有效性。