Nagano Kohji, Taoka Masato, Yamauchi Yoshio, Itagaki Chiharu, Shinkawa Takashi, Nunomura Kazuto, Okamura Nobuko, Takahashi Nobuhiro, Izumi Tomonori, Isobe Toshiaki
Division of Proteomics Research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Proteomics. 2005 Apr;5(5):1346-61. doi: 10.1002/pmic.200400990.
A protein subset expressed in the mouse embryonic stem (ES) cell line, E14-1, was characterized by mass spectrometry-based protein identification technology and data analysis. In total, 1790 proteins including 365 potential nuclear and 260 membrane proteins were identified from tryptic digests of total cell lysates. The subset contained a variety of proteins in terms of physicochemical characteristics, subcellular localization, and biological function as defined by Gene Ontology annotation groups. In addition to many housekeeping proteins found in common with other cell types, the subset contained a group of regulatory proteins that may determine unique ES cell functions. We identified 39 transcription factors including Oct-3/4, Sox-2, and undifferentiated embryonic cell transcription factor I, which are characteristic of ES cells, 88 plasma membrane proteins including cell surface markers such as CD9 and CD81, 44 potential proteinaceous ligands for cell surface receptors including growth factors, cytokines, and hormones, and 100 cell signaling molecules. The subset also contained the products of 60 ES-specific and 41 stemness genes defined previously by the DNA microarray analysis of Ramalho-Santos et al. (Ramalho-Santos et al., Science 2002, 298, 597-600), as well as a number of components characteristic of differentiated cell types such as hematopoietic and neural cells. We also identified potential post-translational modifications in a number of ES cell proteins including five Lys acetylation sites and a single phosphorylation site. To our knowledge, this study provides the largest proteomic dataset characterized to date for a single mammalian cell species, and serves as a basic catalogue of a major proteomic subset that is expressed in mouse ES cells.
利用基于质谱的蛋白质鉴定技术和数据分析,对在小鼠胚胎干细胞系E14 - 1中表达的一个蛋白质亚集进行了表征。从全细胞裂解物的胰蛋白酶消化产物中,总共鉴定出1790种蛋白质,其中包括365种潜在的核蛋白和260种膜蛋白。根据基因本体注释组的定义,该亚集在物理化学特性、亚细胞定位和生物学功能方面包含了多种蛋白质。除了许多与其他细胞类型共有的管家蛋白外,该亚集还包含一组可能决定胚胎干细胞独特功能的调节蛋白。我们鉴定出39种转录因子,包括胚胎干细胞特有的Oct - 3/4、Sox - 2和未分化胚胎细胞转录因子I;88种质膜蛋白,包括细胞表面标志物如CD9和CD81;44种潜在的细胞表面受体蛋白配体,包括生长因子、细胞因子和激素;以及100种细胞信号分子。该亚集还包含先前由Ramalho - Santos等人通过DNA微阵列分析定义的60个胚胎干细胞特异性基因和41个干性基因的产物(Ramalho - Santos等人,《科学》,2002年,298卷,597 - 600页),以及一些分化细胞类型(如造血细胞和神经细胞)特有的成分。我们还在许多胚胎干细胞蛋白质中鉴定出潜在的翻译后修饰,包括五个赖氨酸乙酰化位点和一个磷酸化位点。据我们所知,本研究提供了迄今为止针对单个哺乳动物细胞物种表征的最大蛋白质组数据集,并作为在小鼠胚胎干细胞中表达的主要蛋白质组亚集的基本目录。