Duchardt-Ferner Elke, Juen Michael, Kreutz Christoph, Wöhnert Jens
Institute for Molecular Biosciences, Goethe-University, Frankfurt/M., Max-von-Laue-Str. 9, 60438, Frankfurt, Germany.
Center for Biomolecular Magnetic Resonance (BMRZ), Goethe-University, Frankfurt/M., Max-von-Laue-Str. 9, 60438, Frankfurt, Germany.
Biomol NMR Assign. 2017 Apr;11(1):29-34. doi: 10.1007/s12104-016-9715-6. Epub 2016 Oct 11.
RNA aptamers are used in a wide range of biotechnological or biomedical applications. In many cases the high resolution structures of these aptamers in their ligand-complexes have revealed fundamental aspects of RNA folding and RNA small molecule interactions. Fluorescent RNA-ligand complexes in particular find applications as optical sensors or as endogenous fluorescent tags for RNA tracking in vivo. Structures of RNA aptamers and aptamer ligand complexes constitute the starting point for rational function directed optimization approaches. Here, we present the NMR resonance assignment of an RNA aptamer binding to the fluorescent ligand tetramethylrhodamine (TMR) in complex with the ligand 5-carboxy-tetramethylrhodamine (5-TAMRA) as a starting point for a high-resolution structure determination using NMR spectroscopy in solution.
RNA适体被广泛应用于各种生物技术或生物医学领域。在许多情况下,这些适体与其配体复合物的高分辨率结构揭示了RNA折叠和RNA与小分子相互作用的基本方面。特别是荧光RNA-配体复合物可作为光学传感器或体内RNA追踪的内源性荧光标签。RNA适体及其配体复合物的结构是合理的功能导向优化方法的起点。在这里,我们展示了一种与荧光配体四甲基罗丹明(TMR)结合的RNA适体与配体5-羧基四甲基罗丹明(5-TAMRA)形成复合物的核磁共振共振归属,作为使用溶液核磁共振光谱进行高分辨率结构测定的起点。