Guina Tina, Wu Manhong, Miller Samuel I, Purvine Samuel O, Yi Eugene C, Eng Jimmy, Goodlett David R, Aebersold Ruedi, Ernst Robert K, Lee Kimberly A
Department of Pediatrics, Division of Infectious Diseases, University of Washington, Seattle, Washington 98195, USA.
J Am Soc Mass Spectrom. 2003 Jul;14(7):742-51. doi: 10.1016/S1044-0305(03)00133-8.
In this study, large-scale qualitative and quantitative proteomic technology was applied to the analysis of the opportunistic bacterial pathogen Pseudomonas aeruginosa grown under magnesium limitation, an environmental condition previously shown to induce expression of various virulence factors. For quantitative analysis, whole cell and membrane proteins were differentially labeled with isotope-coded affinity tag (ICAT) reagents and ICAT reagent-labeled peptides were separated by two-dimensional chromatography prior to analysis by electrospray ionization-tandem mass spectrometry (ESI-MS/MS) in an ion trap mass spectrometer (ITMS). To increase the number of protein identifications, gas-phase fractionation (GPF) in the m/z dimension was employed for analysis of ICAT peptides derived from whole cell extracts. The experiments confirmed expression of 1331 P. aeruginosa proteins of which 145 were differentially expressed upon limitation of magnesium. A number of conserved Gram-negative magnesium stress-response proteins involved in bacterial virulence were among the most abundant proteins induced in low magnesium. Comparative ICAT analysis of membrane versus whole cell protein indicated that growth of P. aeruginosa in low magnesium resulted in altered subcellular compartmentalization of large enzyme complexes such as ribosomes. This result was confirmed by 2-D PAGE analysis of P. aeruginosa outer membrane proteins. This study shows that large-scale quantitative proteomic technology can be successfully applied to the analysis of whole bacteria and to the discovery of functionally relevant biologic phenotypes.
在本研究中,大规模定性和定量蛋白质组学技术被应用于分析在镁限制条件下生长的机会性病原菌铜绿假单胞菌,先前已表明这种环境条件会诱导多种毒力因子的表达。对于定量分析,全细胞和膜蛋白用同位素编码亲和标签(ICAT)试剂进行差异标记,ICAT试剂标记的肽在通过离子阱质谱仪(ITMS)进行电喷雾电离串联质谱(ESI-MS/MS)分析之前,先通过二维色谱进行分离。为了增加蛋白质鉴定的数量,在m/z维度上采用气相分级分离(GPF)来分析来自全细胞提取物的ICAT肽。实验证实了1331种铜绿假单胞菌蛋白质的表达,其中145种在镁限制时差异表达。一些参与细菌毒力的保守革兰氏阴性镁应激反应蛋白是在低镁条件下诱导产生的最丰富的蛋白质之一。膜蛋白与全细胞蛋白的比较ICAT分析表明,铜绿假单胞菌在低镁环境中生长会导致大型酶复合物如核糖体的亚细胞区室化发生改变。铜绿假单胞菌外膜蛋白的二维聚丙烯酰胺凝胶电泳(2-D PAGE)分析证实了这一结果。本研究表明,大规模定量蛋白质组学技术可成功应用于全细菌分析及功能相关生物学表型的发现。