Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
J Am Soc Mass Spectrom. 2011 Jun;22(6):989-96. doi: 10.1007/s13361-011-0095-y. Epub 2011 Mar 8.
Protein nitration take place on tyrosine residues under oxidative stress conditions and may influence a number of processes including enzyme activity, protein-protein interactions and phospho-tyrosine signalling pathways. Nitrated proteins have been identified in a number of diseases, however, the study of these proteins has been compromised by the lack of good methods for identifying nitrated proteins, their nitration sites and the level of nitration. Here, we present a method for identification of nitrated peptides that allows the site specific assignment of nitration, is easy to use and reproducible, and opens up for the possibility to quantify the level of nitration of specific peptides as function of different oxidative conditions, namely combined fractional diagonal chromatography (COFRADIC) in combination with off-line nano-LC-MALDI. We identify six nitrated peptides from in vitro nitrated bovine serum albumin and propose that automated COFRADIC using nano-LC and off-line MALDI-MS might be a possibility for identification of tyrosine nitrated proteins and the nitration sites in complex samples.
蛋白质硝化发生在氧化应激条件下的酪氨酸残基上,可能影响包括酶活性、蛋白质-蛋白质相互作用和磷酸酪氨酸信号通路在内的许多过程。已经在许多疾病中鉴定出硝化蛋白质,但是,由于缺乏识别硝化蛋白质、硝化位点和硝化水平的良好方法,这些蛋白质的研究受到了限制。在这里,我们提出了一种鉴定硝化肽的方法,该方法允许对硝化进行特异性分配,易于使用且可重复,并且为定量特定肽的硝化水平提供了可能性,这是作为不同氧化条件的函数,即组合分形对角线色谱(COFRADIC)与离线纳升液相色谱-基质辅助激光解吸/电离质谱联用。我们从体外硝化牛血清白蛋白中鉴定出六个硝化肽,并提出使用纳升液相色谱和离线 MALDI-MS 的自动 COFRADIC 可能是鉴定复杂样品中酪氨酸硝化蛋白质和硝化位点的一种可能性。