Bosch Gundula, Skovran Elizabeth, Xia Qiangwei, Wang Tiansong, Taub Fred, Miller Jonathan A, Lidstrom Mary E, Hackett Murray
Department of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.
Proteomics. 2008 Sep;8(17):3494-505. doi: 10.1002/pmic.200800152.
In order to validate a gel free quantitative proteomics assay for the model methylotrophic bacterium Methylobacterium extorquens AM1, we examined the M. extorquens AM1 proteome under single carbon (methanol) and multicarbon (succinate) growth, conditions that have been studied for decades and for which extensive corroborative data have been compiled. In total, 4447 proteins from a database containing 7556 putative ORFs from M. extorquens AM1 could be identified with two or more peptide sequences, corresponding to a qualitative proteome coverage of 58%. Statistically significant nonzero (log(2) scale) differential abundance ratios of methanol/succinate could be detected for 317 proteins using summed ion intensity measurements and 585 proteins using spectral counting, at a q-value cut-off of 0.01, a measure of false discovery rate. The results were compared to recent microarray studies performed under equivalent chemostat conditions. The M. extorquens AM1 studies demonstrated the feasibility of scaling up the multidimensional capillary HPLC MS/MS approach to a prokaryotic organism with a proteome more than three times the size of microbes we have investigated previously, while maintaining a high degree of proteome coverage and reliable quantitative abundance ratios.
为了验证适用于模式甲基营养菌嗜甲基甲基杆菌AM1的无凝胶定量蛋白质组学分析方法,我们研究了嗜甲基甲基杆菌AM1在单碳(甲醇)和多碳(琥珀酸)生长条件下的蛋白质组,这些条件已被研究数十年且积累了大量的确证数据。总共可以从一个包含嗜甲基甲基杆菌AM1的7556个推定开放阅读框的数据库中鉴定出4447种蛋白质,其具有两个或更多的肽序列,对应的定性蛋白质组覆盖率为58%。使用总离子强度测量方法,在q值截止为0.01(一种错误发现率的度量)时,可以检测到317种蛋白质的甲醇/琥珀酸的统计学上显著的非零(对数(2)尺度)差异丰度比;使用光谱计数法,可以检测到585种蛋白质的该差异丰度比。将结果与在等效恒化器条件下进行的近期微阵列研究进行了比较。嗜甲基甲基杆菌AM1的研究证明了将多维毛细管HPLC MS/MS方法扩大应用于一种蛋白质组比我们之前研究的微生物大三倍以上的原核生物的可行性,同时保持了高度的蛋白质组覆盖率和可靠的定量丰度比。