Forbus Jeffery, Spratt Heidi, Wiktorowicz John, Wu Zheng, Boldogh Istvan, Denner Larry, Kurosky Alexander, Brasier Robert C, Luxon Bruce, Brasier Allan R
Department of Medicine, The University of Texas Medical Branch, Galveston, TX 77555-1060, USA.
Proteomics. 2006 May;6(9):2656-72. doi: 10.1002/pmic.200500652.
The airway epithelial cell plays a central role in coordinating airway inflammatory responses, where significant changes in the proteome occur in response to infectious stimuli. To further understand the spectrum of proteins and the biological processes they control, we have initially determined the nuclear proteome of human type II-like alveolar epithelial cells (A549) using a sequential method of organellar enrichment followed by HPLC prefractionation prior to 2-DE-based protein identification using MALDI-TOF MS. This approach yielded 719 high-confidence identifications, 433 mapping to unique gene identifiers. Expert classification showed that these proteins controlled chromatin remodeling, protein refolding, cytoskeletal structure, membrane function, metabolic processes, mitochondrial function, RNA binding, protein synthesis, signaling, and transcription factor activities. The proteins were mapped to gene ontology classifications, where metabolism and catalytic activity functions were significantly enriched, representing 43 and 32% of the protein set, respectively. Pathways analysis indicated a protein network affecting tumor necrosis factor-nuclear factor-kappaB signaling pathway interacting with intermediate cytoskeletal filaments. Forty-five proteins of unknown function were subjected to domain analysis and inferred to have additional nuclear functions controlling purine nucleotide metabolism and protein-protein interactions. This database represents the most comprehensive data set of mammalian nuclear proteins and will serve as a foundation for further discovery.
气道上皮细胞在协调气道炎症反应中起核心作用,在感染性刺激下蛋白质组会发生显著变化。为了进一步了解蛋白质谱及其所控制的生物学过程,我们首先采用细胞器富集的顺序方法,随后进行HPLC预分级,然后基于二维电泳使用MALDI-TOF MS进行蛋白质鉴定,确定了人II型肺泡上皮细胞(A549)的核蛋白质组。这种方法产生了719个高可信度鉴定结果,其中433个映射到唯一的基因标识符。专家分类表明,这些蛋白质控制染色质重塑、蛋白质重折叠、细胞骨架结构、膜功能、代谢过程、线粒体功能、RNA结合、蛋白质合成、信号传导和转录因子活性。这些蛋白质被映射到基因本体分类中,其中代谢和催化活性功能显著富集,分别占蛋白质组的43%和32%。通路分析表明,一个影响肿瘤坏死因子-核因子-κB信号通路的蛋白质网络与中间细胞骨架丝相互作用。对45个功能未知的蛋白质进行了结构域分析,并推断它们具有控制嘌呤核苷酸代谢和蛋白质-蛋白质相互作用的额外核功能。该数据库代表了最全面的哺乳动物核蛋白质数据集,将为进一步的发现奠定基础。