核酶
发夹状核酶
核糖开关
化学
质子化
基质(水族馆)
环氧化物
核糖核酸
立体化学
鸟嘌呤
核酶
化学生物学
连接酶核酶
小分子
组合化学
作者
Daniel Krochmal,Yaming Shao,Nan-Sheng Li,Saurja DasGupta,Sandip A. Shelke,Deepak Koirala,Joseph A. Piccirilli
标识
DOI:10.1038/s41589-021-00950-z
摘要
Ribozymes that react with small-molecule probes have important applications in transcriptomics and chemical biology, such as RNA labeling and imaging. Understanding the structural basis for these RNA-modifying reactions will enable the development of better tools for studying RNA. Nevertheless, high-resolution structures and underlying catalytic mechanisms for members of this ribozyme class remain elusive. Here, we focus on a self-alkylating ribozyme that catalyzes nitrogen-carbon bond formation between a specific guanine and a 2,3-disubstituted epoxide substrate and report the crystal structures of a self-alkylating ribozyme, including both alkylated and apo forms, at 1.71-Å and 2.49-Å resolution, respectively. The ribozyme assumes an elongated hairpin-like architecture preorganized to accommodate the epoxide substrate in a hook-shaped conformation. Observed reactivity of substrate analogs together with an inverse, log-linear pH dependence of the reaction rate suggests a requirement for epoxide protonation, possibly assisted by the ether oxygens within the substrate.
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