Barrick J E, Takahashi T T, Balakin A, Roberts R W
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Methods. 2001 Mar;23(3):287-93. doi: 10.1006/meth.2000.1139.
We have been working to apply in vitro selection to isolate novel RNA-binding peptides. To do this, we use mRNA-protein fusions, peptides covalently attached to their own mRNA. Here, we report selection protocols developed using the arginine-rich domain of bacteriophage lambda-N protein and its binding target, the boxB RNA. Systematic investigation of possible paths for a selection round has allowed us to design a reliable and efficient protocol to enrich RNA-binding peptides from nonfunctional members of a complex mixture. The protocols we have developed should greatly facilitate the isolation of new molecules using the fusion system.
我们一直在致力于应用体外筛选技术来分离新型RNA结合肽。为此,我们使用mRNA-蛋白质融合体,即与自身mRNA共价连接的肽。在此,我们报告了利用噬菌体λ-N蛋白的富含精氨酸结构域及其结合靶点boxB RNA开发的筛选方案。对筛选轮次可能路径的系统研究使我们能够设计出一种可靠且高效的方案,以从复杂混合物的无功能成员中富集RNA结合肽。我们开发的方案应极大地促进使用融合系统分离新分子。