Couto Narciso, Schooling Sarah R, Dutcher John R, Barber Jill
Michael Barber Centre for Mass Spectrometry, Manchester Institute for Biotechnology, University of Manchester , Princess Road, Manchester, M1 7DN, U.K.
Department of Molecular and Cellular Biology, College of Biological Science, University of Guelph , Guelph, ON N1G 2W1, Canada.
J Proteome Res. 2015 Oct 2;14(10):4207-22. doi: 10.1021/acs.jproteome.5b00312. Epub 2015 Sep 15.
In the present work, two different proteomic platforms, gel-based and gel-free, were used to map the matrix and outer membrane vesicle exoproteomes of Pseudomonas aeruginosa PAO1 biofilms. These two proteomic strategies allowed us a confident identification of 207 and 327 proteins from enriched outer membrane vesicles and whole matrix isolated from biofilms. Because of the physicochemical characteristics of these subproteomes, the two strategies showed complementarity, and thus, the most comprehensive analysis of P. aeruginosa exoproteome to date was achieved. Under our conditions, outer membrane vesicles contribute approximately 20% of the whole matrix proteome, demonstrating that membrane vesicles are an important component of the matrix. The proteomic profiles were analyzed in terms of their biological context, namely, a biofilm. Accordingly relevant metabolic processes involved in cellular adaptation to the biofilm lifestyle as well as those related to P. aeruginosa virulence capabilities were a key feature of the analyses. The diversity of the matrix proteome corroborates the idea of high heterogeneity within the biofilm; cells can display different levels of metabolism and can adapt to local microenvironments making this proteomic analysis challenging. In addition to analyzing our own primary data, we extend the analysis to published data by other groups in order to deepen our understanding of the complexity inherent within biofilm populations.
在本研究中,使用了两种不同的蛋白质组学平台,即基于凝胶和非凝胶的平台,来绘制铜绿假单胞菌PAO1生物膜的基质和外膜囊泡外蛋白质组图谱。这两种蛋白质组学策略使我们能够可靠地鉴定出从生物膜中分离出的富集外膜囊泡和整个基质中的207种和327种蛋白质。由于这些亚蛋白质组的物理化学特性,这两种策略显示出互补性,因此实现了迄今为止对铜绿假单胞菌外蛋白质组最全面的分析。在我们的条件下,外膜囊泡约占整个基质蛋白质组的20%,表明膜囊泡是基质的重要组成部分。根据其生物学背景,即生物膜,对蛋白质组图谱进行了分析。因此,参与细胞适应生物膜生活方式以及与铜绿假单胞菌毒力相关的相关代谢过程是分析的关键特征。基质蛋白质组的多样性证实了生物膜内高度异质性的观点;细胞可以表现出不同水平的代谢,并能适应局部微环境,这使得这种蛋白质组分析具有挑战性。除了分析我们自己的原始数据外,我们还将分析扩展到其他小组发表的数据,以加深我们对生物膜群体内在复杂性的理解。