Welty Robb, Hall Kathleen B
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Mol Biol. 2016 Nov 6;428(22):4490-4502. doi: 10.1016/j.jmb.2016.09.015. Epub 2016 Sep 29.
The tertiary structure of the GTPase center (GAC) of 23S ribosomal RNA (rRNA) as seen in cocrystals is extremely compact. It is stabilized by long-range hydrogen bonds and nucleobase stacking and by a triloop that forms within its three-way junction. Its folding pathway from secondary structure to tertiary structure has not been previously observed, but it was shown to require Mg ions in equilibrium experiments. The fluorescent nucleotide 2-aminopurine was substituted at selected sites within the 60-nt GAC. Fluorescence intensity changes upon addition of MgCl were monitored over a time-course from 1ms to 100s as the RNA folds. The folding pathway is revealed here to be hierarchical through several intermediates. Observation of the nucleobases during folding provides a new perspective on the process and the pathway, revealing the dynamics of nucleobase conformational exchange during the folding transitions.
在共晶体中观察到的23S核糖体RNA(rRNA)的GTPase中心(GAC)的三级结构极其紧凑。它通过长程氢键和核碱基堆积以及在其三岔路口形成的三链环来稳定。其从二级结构到三级结构的折叠途径以前未曾观察到,但在平衡实验中表明它需要镁离子。荧光核苷酸2-氨基嘌呤被取代在60个核苷酸的GAC内的选定位点。当RNA折叠时,在从1毫秒到100秒的时间进程中监测添加MgCl后荧光强度的变化。此处揭示的折叠途径是通过几个中间体分层进行的。在折叠过程中对核碱基的观察为该过程和途径提供了新的视角,揭示了折叠转变过程中核碱基构象交换的动态变化。