Korostelev Andrei, Noller Harry F
Center for Molecular Biology of RNA and Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.
Trends Biochem Sci. 2007 Sep;32(9):434-41. doi: 10.1016/j.tibs.2007.08.002. Epub 2007 Aug 30.
Recent all-atom crystal structures of 70S ribosome functional complexes provide a detailed description of how the ribosome interacts with its mRNA and tRNA substrates. The structures support the view that the fundamental steps of translation are based on RNA-RNA interactions, which in some cases underwent further refinement as a result of having recruited proteins. The structural basis of the discrimination of cognate tRNA, the high affinity for tRNA in the peptidyl-tRNA site, the structure of the peptidyl transferase catalytic center, the specificity of the exit site for deacylated tRNA and other functional properties of the ribosome are now explained, confirmed or visualized for the first time in complexes containing full-length tRNAs and defined mRNAs. Clues to the structural dynamics of translation are suggested by conformational changes that occur in both tRNA and the ribosome upon complex formation.
近期70S核糖体功能复合物的全原子晶体结构详细描述了核糖体如何与mRNA和tRNA底物相互作用。这些结构支持了这样一种观点,即翻译的基本步骤基于RNA-RNA相互作用,在某些情况下,由于招募了蛋白质,这种相互作用得到了进一步完善。在含有全长tRNA和特定mRNA的复合物中,首次解释、证实或可视化了同源tRNA识别的结构基础、肽基-tRNA位点对tRNA的高亲和力、肽基转移酶催化中心的结构、脱酰基tRNA出口位点的特异性以及核糖体的其他功能特性。复合物形成时tRNA和核糖体中发生的构象变化暗示了翻译结构动力学的线索。