Department of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland 21202, United States.
J Proteome Res. 2020 Sep 4;19(9):3708-3715. doi: 10.1021/acs.jproteome.0c00245. Epub 2020 Jun 17.
Fast photochemical oxidation of proteins (FPOP) is a hydroxyl radical protein footprinting method that covalently labels solvent-accessible amino acids by photolysis of hydrogen peroxide. Recently, we expanded the use of FPOP for (IV-FPOP) covalent labeling in . In initial IV-FPOP studies, 545 proteins were oxidatively modified in all body systems within the worm. Here, with the use of chemical penetration enhancers (CPEs), we increased the number of modified proteins as well as the number of modifications per protein to gain more structural information. CPEs aid in the delivery of hydrogen peroxide inside by disturbing the highly ordered lipid bilayer of the worm cuticle without affecting worm viability. IV-FPOP experiments performed using the CPE azone showed an increase in oxidatively modified proteins and peptides. This increase correlated with greater hydrogen peroxide uptake by quantified using a chemical fluorophore demonstrating the efficacy of using CPEs with IV-FPOP. Mass spectrometry proteomics data are available via ProteomeXchange with identifier PXD019290.
快速光化学氧化蛋白质(FPOP)是一种羟基自由基蛋白质足迹法,通过光解过氧化氢共价标记可及溶剂的氨基酸。最近,我们扩展了 FPOP 的用途,用于线虫体内的(IV-FPOP)共价标记。在最初的 IV-FPOP 研究中,在虫体的所有身体系统中氧化修饰了 545 种蛋白质。在这里,我们使用化学渗透增强剂(CPE),通过扰乱虫体角质层高度有序的脂质双层而不影响虫体活力,增加了修饰蛋白的数量以及每个蛋白的修饰数量,以获得更多的结构信息。CPE 有助于通过扰乱虫体角质层高度有序的脂质双层而不影响虫体活力,将过氧化氢递送至虫体内。使用 CPE 氮酮进行的 IV-FPOP 实验显示,氧化修饰的蛋白质和肽增加。这种增加与使用化学荧光探针定量的通过虫体的过氧化氢摄取量增加相关,这证明了使用 CPE 与 IV-FPOP 结合的有效性。质谱蛋白质组学数据可通过 ProteomeXchange 以标识符 PXD019290 获取。