Biophysics Program, Stanford University, Stanford, California 94305-5126, USA.
Annu Rev Biophys. 2010;39:491-513. doi: 10.1146/annurev.biophys.093008.131427.
Our current understanding of the mechanism of translation is based on nearly fifty years of biochemical and biophysical studies. This mechanism, which requires the ribosome to manipulate tRNA and step repetitively along the mRNA, implies movement. High-resolution structures of the ribosome and its ligands have recently described translation in atomic detail, capturing the endpoints of large-scale rearrangements of the ribosome. Direct observation of the dynamic events that underlie the mechanism of translation is challenged by ensemble averaging in bulk solutions. Single-molecule methods, which eliminate these averaging effects, have emerged as powerful tools to probe the mechanism of translation. Single-molecule fluorescence experiments have described the dynamic motion of the ribosome and tRNA. Single-molecule force measurements have directly probed the forces stabilizing ribosomal complexes. Recent developments have allowed real-time observation of ribosome movement and dynamics during translation. This review covers the contributions of single-molecule studies to our understanding of the dynamic nature of translation.
我们目前对翻译机制的理解是基于近五十年来的生化和生物物理研究。这种机制需要核糖体来操纵 tRNA 并沿着 mRNA 重复移动,这意味着需要移动。核糖体及其配体的高分辨率结构最近以原子细节描述了翻译过程,捕捉到了核糖体大规模重排的终点。在批量溶液中进行的整体平均会对直接观察翻译机制背后的动态事件构成挑战。消除这些平均效应的单分子方法已成为探测翻译机制的强大工具。单分子荧光实验已经描述了核糖体和 tRNA 的动态运动。单分子力测量直接探测稳定核糖体复合物的力。最近的发展使得在翻译过程中实时观察核糖体的运动和动态成为可能。这篇综述涵盖了单分子研究对我们理解翻译动态性质的贡献。