核糖核酸
堆积
折叠(DSP实现)
毫秒
核酸结构
核酸
碱基对
螺旋(腹足类)
高分子
分辨率(逻辑)
DNA
生物物理学
埃
物理
化学
结晶学
生物
计算机科学
生物化学
基因
量子力学
电气工程
蜗牛
核磁共振
生态学
工程类
人工智能
作者
Kara A. Zielinski,Shuo Sui,Suzette A. Pabit,Daniel Rivera,Tong Wang,Qingyue Hu,M.M. Kashipathy,Stella Lisova,Chris B. Schaffer,Valerio Mariani,Mark S. Hunter,Christopher Kupitz,Frank R. Moss,Frédéric Poitevin,Thomas D. Grant,Lois Pollack
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-09-27
卷期号:9 (39): eadj3509-eadj3509
被引量:11
标识
DOI:10.1126/sciadv.adj3509
摘要
RNA macromolecules, like proteins, fold to assume shapes that are intimately connected to their broadly recognized biological functions; however, because of their high charge and dynamic nature, RNA structures are far more challenging to determine. We introduce an approach that exploits the high brilliance of x-ray free-electron laser sources to reveal the formation and ready identification of angstrom-scale features in structured and unstructured RNAs. Previously unrecognized structural signatures of RNA secondary and tertiary structures are identified through wide-angle solution scattering experiments. With millisecond time resolution, we observe an RNA fold from a dynamically varying single strand through a base-paired intermediate to assume a triple-helix conformation. While the backbone orchestrates the folding, the final structure is locked in by base stacking. This method may help to rapidly characterize and identify structural elements in nucleic acids in both equilibrium and time-resolved experiments.
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