Howard Hughes Medical Institute, Department of Biochemistry and Molecular Biophysics, Columbia University, 650 W. 168th Street, New York, NY 10032, United States.
Curr Opin Struct Biol. 2012 Dec;22(6):778-85. doi: 10.1016/j.sbi.2012.08.001. Epub 2012 Aug 17.
Recent studies support the notion that the pre-translocation (PRE) ribosomal complex functions, at least in part, as a Brownian machine, stochastically fluctuating among multiple conformations and transfer RNA (tRNA) binding configurations. Apart from the relatively more energetically stable conformational states of the PRE complex, termed macrostate I (MS I) and macrostate II (MS II), several additional intermediate states have been recently discovered. Structural and kinetic analyses of these states, made possible by cryogenic-electron microscopy (cryo-EM), X-ray crystallography, and single-molecule fluorescence resonance energy transfer (smFRET), have provided important insights into the translocation process, which is now understood to proceed, at least in the first step of the process, as a Brownian machine that is transiently stabilized in the 'productive' MS II conformation by the binding of the translocase elongation factor G (EF-G).
最近的研究支持这样一种观点,即前转移(PRE)核糖体复合物至少部分充当布朗机,在多种构象和转移 RNA(tRNA)结合构象之间随机波动。除了 PRE 复合物的相对更具能量稳定性的构象状态,称为宏观状态 I(MS I)和宏观状态 II(MS II)外,最近还发现了几个额外的中间状态。通过低温电子显微镜(cryo-EM)、X 射线晶体学和单分子荧光共振能量转移(smFRET)进行的这些状态的结构和动力学分析,为转移过程提供了重要的见解,现在人们理解该过程至少在第一步中作为布朗机进行,该布朗机通过易位酶伸长因子 G(EF-G)的结合而在“有生产力的”MS II 构象中短暂稳定。