Kazuta Yasuaki, Adachi Jiro, Matsuura Tomoaki, Ono Naoaki, Mori Hirotada, Yomo Tetsuya
Department of Bioinformatics Engineering, Osaka University, Japan.
Mol Cell Proteomics. 2008 Aug;7(8):1530-40. doi: 10.1074/mcp.M800051-MCP200. Epub 2008 May 2.
Protein synthesis is one of the most important reactions in the cell. Recent experimental studies indicated that this complex reaction can be achieved with a minimum complement of 36 proteins and ribosomes by reconstituting an Escherichia coli-based in vitro translation system with these protein components highly purified on an individual basis. From the protein-protein interaction (PPI) network of E. coli proteins, these minimal protein components are known to interact physically with large numbers of proteins. However, it is unclear what fraction of E. coli proteins are linked functionally with the minimal protein synthesis system. We investigated the effects of each of the 4194 E. coli ORF products on the minimal protein synthesis system; at least 12% of the entire ORF products, a significant fraction of the gene product of E. coli, affect the activity of this system. Furthermore 34% of these functional modifiers present in the PPI network were shown by mapping to be directly linked (i.e. to interact physically) with the minimal components of the PPI network. Topological analysis of the relationships between modifiers and the minimal components in the PPI network indicated clustering of the minimal components. The modifiers showed no such clustering, indicating that the location of functional modifiers is spread across the PPI network rather than clustering close to the minimal protein components. These observations may reflect the evolutionary process of the protein synthesis system.
蛋白质合成是细胞中最重要的反应之一。最近的实验研究表明,通过用逐个高度纯化的蛋白质组分重建基于大肠杆菌的体外翻译系统,仅需最少36种蛋白质和核糖体就能实现这一复杂反应。从大肠杆菌蛋白质的蛋白质 - 蛋白质相互作用(PPI)网络可知,这些最小蛋白质组分与大量蛋白质存在物理相互作用。然而,尚不清楚大肠杆菌中有多少比例的蛋白质与最小蛋白质合成系统存在功能联系。我们研究了4194种大肠杆菌开放阅读框(ORF)产物中的每一种对最小蛋白质合成系统的影响;至少12%的全部ORF产物(这是大肠杆菌基因产物的相当一部分)会影响该系统的活性。此外,通过图谱分析表明,PPI网络中34%的这些功能修饰因子与PPI网络的最小组分直接相连(即存在物理相互作用)。对PPI网络中修饰因子与最小组分之间关系的拓扑分析表明,最小组分存在聚类现象。修饰因子则没有这种聚类现象,这表明功能修饰因子的位置分布在整个PPI网络中,而非聚集在最小蛋白质组分附近。这些观察结果可能反映了蛋白质合成系统的进化过程。