Real-time multidimensional NMR follows RNA folding with second resolution

被引:92
作者
Lee, Mi-Kyung [2 ]
Gal, Maayan [1 ]
Frydman, Lucio [1 ]
Varani, Gabriele [2 ,3 ]
机构
[1] Weizmann Inst Sci, Dept Chem Phys, IL-76100 Rehovot, Israel
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[3] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
基金
美国国家卫生研究院; 以色列科学基金会;
关键词
dynamics; riboswitches; ultrafast NMR; conformational transition; ADENINE-SENSING RIBOSWITCH; NUCLEAR-MAGNETIC-RESONANCE; PROTEIN RECOGNITION; GENE-EXPRESSION; LIGAND-BINDING; APTAMER DOMAIN; INDUCED FIT; SPECTROSCOPY; SPECIFICITY; ACQUISITION;
D O I
10.1073/pnas.1001195107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Conformational transitions and structural rearrangements are central to the function of many RNAs yet remain poorly understood. We have used ultrafast multidimensional NMR techniques to monitor the adenine-induced folding of an adenine-sensing riboswitch in real time, with nucleotide-resolved resolution. By following changes in 2D spectra at rates of approximately 0.5 Hz, we identify distinct steps associated with the ligand-induced folding of the riboswitch. Following recognition of the ligand, long range loop-loop interactions form and are then progressively stabilized before the formation of a fully stable complex over approximately 2-3 minutes. The application of these ultrafast multidimensional NMR methods provides the opportunity to determine the structure of RNA folding intermediates and conformational trajectories.
引用
收藏
页码:9192 / 9197
页数:6
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