Brill Laurence M, Motamedchaboki Khatereh, Wu Shuangding, Wolf Dieter A
NCI Cancer Center Proteomics Facility, Burnham Institute for Medical Research, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Methods. 2009 Jul;48(3):311-9. doi: 10.1016/j.ymeth.2009.02.023. Epub 2009 Mar 9.
We describe a detailed and widely applicable method for comprehensive proteomic profiling of the fission yeast Schizosaccharomyces pombe by 2-dimensional high performance liquid chromatography-electrospray ionization-tandem mass spectrometry that demonstrates high sensitivity and robust operation. Steps ranging from the preparation of total proteins, digestion of proteins to peptides, and separation of peptides by two-dimensional (1. strong cation exchange and 2. reversed-phase) high performance liquid chromatography followed by tandem mass spectrometry and data processing have been optimized for our instrumentation platform. Using this technology, we identify ca. 3400 proteins per sample and have identified an estimated 4600 proteins in vegetative cells (equal to ca. 90% of the predicted S. pombe proteome) at a false discovery rate of 0.02. Considering the fact that approximately 500 genes are strongly induced during sexual differentiation, and sexual differentiation was not included in our experiments, the proteomic profiling technique affords what should be virtually complete coverage of the vegetative S. pombe proteome. In addition, these methods are widely applicable, having been used for proteomic profiling of several other organisms.
我们描述了一种详细且广泛适用的方法,用于通过二维高效液相色谱 - 电喷雾电离 - 串联质谱对裂殖酵母粟酒裂殖酵母进行全面蛋白质组分析,该方法具有高灵敏度和稳健的操作性。从总蛋白制备、蛋白质消化成肽段,到通过二维(1. 强阳离子交换和2. 反相)高效液相色谱分离肽段,随后进行串联质谱分析和数据处理等步骤,均已针对我们的仪器平台进行了优化。使用该技术,我们每个样品可鉴定约3400种蛋白质,并且在错误发现率为0.02的情况下,已在营养细胞中鉴定出约4600种蛋白质(约占预测的粟酒裂殖酵母蛋白质组的90%)。考虑到在有性分化过程中约有500个基因被强烈诱导,且我们的实验未包括有性分化,该蛋白质组分析技术几乎能完全覆盖营养型粟酒裂殖酵母的蛋白质组。此外,这些方法具有广泛的适用性,已用于其他几种生物的蛋白质组分析。