Yang Y, Kochoyan M, Burgstaller P, Westhof E, Famulok M
Centre de Biochimie Structurale (CBS), Unité Mixte de Recherche, CNRS 9955, Montpellier, France.
Science. 1996 May 31;272(5266):1343-7. doi: 10.1126/science.272.5266.1343.
In a previous study, an RNA aptamer for the specific recognition of arginine was evolved from a parent sequence that bound citrulline specifically. The two RNAs differ at only 3 positions out of 44. The solution structures of the two aptamers complexed to their cognate amino acids have now been determined by two-dimensional nuclear magnetic resonance spectroscopy. Both aptamers contain two asymmetrical internal loops that are not well ordered in the free RNA but that fold into a compact structure upon ligand binding. Those nucleotides common to both RNAs include a conserved cluster of purine residues, three of which form an uneven plane containing a G:G pair, and two other residues nearly perpendicular to that surface. Two of the three variant nucleotides are stacked on the cluster of purines and form a triple contact to the amino acid side chain, whereas the edge of the third variant nucleotide is capping the binding pocket.
在之前的一项研究中,一种用于特异性识别精氨酸的RNA适配体是从一个能特异性结合瓜氨酸的亲本序列进化而来的。这两种RNA在44个位置中只有3个位置不同。现在已经通过二维核磁共振光谱法确定了与它们各自的同源氨基酸复合的两种适配体的溶液结构。两种适配体都包含两个不对称的内部环,这些环在游离RNA中排列不规则,但在配体结合时会折叠成紧密结构。两种RNA共有的那些核苷酸包括一组保守的嘌呤残基,其中三个形成一个包含G:G对的不平坦平面,另外两个残基几乎垂直于该表面。三个变异核苷酸中的两个堆积在嘌呤簇上,并与氨基酸侧链形成三重接触,而第三个变异核苷酸的边缘则覆盖着结合口袋。