Natsume Tohru, Yamauchi Yoshio, Nakayama Hiroshi, Shinkawa Takashi, Yanagida Mitsuaki, Takahashi Nobuhiro, Isobe Toshiaki
Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Japan.
Anal Chem. 2002 Sep 15;74(18):4725-33. doi: 10.1021/ac020018n.
One of the strategies of functional proteomics, research aiming to discover gene function at the protein level, is the comprehensive analysis of protein-protein interactions related to the functional linkage among proteins and analysis of functional cellular machinery to better understand the basis of cell functions. Here, we describe the direct nanoflow LC (DNLC) system, which is equipped with a fritless high-resolution electrospray interface column packed with 1-microm reversed-phase (RP) beads and a novel splitless nanoflow gradient elution system to operate the column. Using RP-DNLC at an extremely slow flow rate, <50 nL/min, combined with data-dependent collision-induced dissociation tandem MS (MS/MS) and computer-assisted retrieval of spectra, we identified approximately 100 protein components in a biological complex such as a premature mammalian ribosome pull-down from cultured cells when we used an epitope-tagged protein as bait. Because this analysis is most sensitive, requires approximately 0.2 microg of total protein, and is a fully automated 1-h process, we anticipated that it should be an excellent tool for analyzing a limited amount of functional multi-protein complexes in cells.
功能蛋白质组学旨在在蛋白质水平上发现基因功能,其策略之一是全面分析与蛋白质功能联系相关的蛋白质-蛋白质相互作用,并分析功能性细胞机制,以更好地理解细胞功能的基础。在此,我们描述了直接纳流液相色谱(DNLC)系统,该系统配备了填充有1微米反相(RP)珠子的无 frit 高分辨率电喷雾接口柱和用于操作该柱的新型不分流纳流梯度洗脱系统。使用流速极慢(<50 nL/min)的RP-DNLC,结合数据依赖的碰撞诱导解离串联质谱(MS/MS)和计算机辅助光谱检索,当我们使用表位标签蛋白作为诱饵时,我们在从培养细胞中拉下的早熟哺乳动物核糖体等生物复合物中鉴定出了约100种蛋白质成分。由于这种分析灵敏度极高,总共需要约0.2微克蛋白质,且是一个完全自动化的1小时过程,我们预计它应该是分析细胞中有限量功能性多蛋白复合物的极佳工具。