Jiang F, Kumar R A, Jones R A, Patel D J
Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York 10021, USA.
Nature. 1996 Jul 11;382(6587):183-6. doi: 10.1038/382183a0.
The catalytic properties of RNA and its well known role in gene expression and regulation are the consequence of its unique solution structures. Identification of the structural determinants of ligand recognition by RNA molecules is of fundamental importance for understanding the biological functions of RNA, as well as for the rational design of RNA Sequences with specific catalytic activities. Towards this latter end, Szostak et al. used in vitro selection techniques to isolate RNA sequences ('aptamers') containing a high-affinity binding site for ATP, the universal currency of cellular energy, and then used this motif to engineer ribozymes with polynucleotide kinase activity. Here we present the solution structure, as determined by multidimensional NMR spectroscopy and molecular dynamics calculations, of both uniformly and specifically 13C-, 15N-labelled 40-mer RNA containing the ATP-binding motif complexed with AMP. The aptamer adopts an L-shaped structure with two nearly orthogonal stems, each capped proximally by a G x G mismatch pair, binding the AMP ligand at their junction in a GNRA-like motif.
RNA的催化特性及其在基因表达和调控中广为人知的作用是其独特溶液结构的结果。确定RNA分子识别配体的结构决定因素对于理解RNA的生物学功能以及合理设计具有特定催化活性的RNA序列至关重要。为了实现后一个目标,绍斯塔克等人使用体外筛选技术分离出对细胞能量的通用货币ATP具有高亲和力结合位点的RNA序列(“适体”),然后利用这个基序设计具有多核苷酸激酶活性的核酶。在此,我们展示了通过多维核磁共振光谱和分子动力学计算确定的,与AMP复合的含有ATP结合基序的均匀且特异性13C、15N标记的40聚体RNA的溶液结构。该适体采用L形结构,有两个近乎正交的茎,每个茎在近端由一个G×G错配碱基对封端,并以类似GNRA的基序在它们的交界处结合AMP配体。