Sasaki Hiroshi M, Tadakuma Hisashi, Tomari Yukihide
Intsitute for Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, 113-0032, Japan.
Wyss Institute for Biologically Inspired Engineering, Harvard University, 3 Blackfan Circle, CLSB, Boston, MA, 02115, USA.
Methods Mol Biol. 2018;1680:145-164. doi: 10.1007/978-1-4939-7339-2_10.
RNA-induced silencing complex (RISC) is a small RNA-protein complex that mediates silencing of complementary target RNAs. Biochemistry has been successfully used to characterize the molecular mechanism of RISC assembly and function for nearly two decades. However, further dissection of intermediate states during the reactions has been warranted to fill in the gaps in our understanding of RNA silencing mechanisms. Single-molecule analysis with total internal reflection fluorescence (TIRF) microscopy is a powerful imaging-based approach to interrogate complex formation and dynamics at the individual molecule level with high sensitivity. Combining this technique with our recently established in vitro reconstitution system of fly Ago2-RISC, we have developed a single-molecule observation system for RISC assembly. In this chapter, we summarize the detailed protocol for single-molecule analysis of chaperone-assisted assembly of fly Ago2-RISC as well as its target cleavage reaction.
RNA诱导沉默复合体(RISC)是一种小RNA-蛋白质复合体,介导互补靶RNA的沉默。近二十年来,生物化学已成功用于表征RISC组装和功能的分子机制。然而,有必要进一步剖析反应过程中的中间状态,以填补我们对RNA沉默机制理解上的空白。全内反射荧光(TIRF)显微镜的单分子分析是一种强大的基于成像的方法,能够在单分子水平上以高灵敏度研究复合物的形成和动力学。将该技术与我们最近建立的果蝇Ago2-RISC体外重组系统相结合,我们开发了一种用于RISC组装的单分子观察系统。在本章中,我们总结了果蝇Ago2-RISC伴侣蛋白辅助组装及其靶切割反应的单分子分析详细方案。