Nieuwlandt D, Wecker M, Gold L
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309, USA.
Biochemistry. 1995 Apr 25;34(16):5651-9. doi: 10.1021/bi00016a041.
RNA ligands to the tachykinin substance P have been selected from a large pool of random sequence RNA molecules. Substance P is an undecapeptide that plays a variety of roles as a neurotransmitter and neuromodulator in the central and peripheral nervous system of mammals. A systematic evolution of ligands by exponential enrichment (SELEX) procedure was used to isolate RNAs that bind substance P immobilized on a solid support. RNAs that also bind substance P in solution were identified, and the tightest binder was subjected to mutagenesis in a second SELEX procedure to evolve ligands with a higher affinity for the peptide. A comparative analysis of 36 ligands isolated from the second SELEX experiment revealed two main sequence classes with highly conserved secondary structures within each class. Dissociation constants for the interaction of these ligands with substance P in solution were determined by equilibrium dialysis. The amino acid residues involved in the interaction with the highest affinity ligand (190 nM Kd) were mapped by determining which of a set of overlapping fragments of substance P can compete with the intact peptide for binding. A binding competition experiment also demonstrated the ability of the same ligand to discriminate between substance P and the reverse orientation of the same amino acid sequence. The results from this study demonstrate that SELEX can yield high affinity RNA ligands to small nonconstrained peptides.
已从大量随机序列RNA分子中筛选出速激肽P物质的RNA配体。P物质是一种十一肽,在哺乳动物的中枢和外周神经系统中作为神经递质和神经调节剂发挥多种作用。采用指数富集配体系统进化(SELEX)程序来分离与固定在固体支持物上的P物质结合的RNA。鉴定出在溶液中也能与P物质结合的RNA,并在第二个SELEX程序中对结合最紧密的RNA进行诱变,以进化出对该肽具有更高亲和力的配体。对从第二个SELEX实验中分离出的36种配体的比较分析揭示了两个主要的序列类别,每个类别内具有高度保守的二级结构。通过平衡透析测定这些配体与溶液中P物质相互作用的解离常数。通过确定P物质的一组重叠片段中的哪一个可以与完整肽竞争结合,来绘制与最高亲和力配体(Kd为190 nM)相互作用的氨基酸残基。结合竞争实验还证明了同一配体区分P物质和相同氨基酸序列反向排列的能力。这项研究的结果表明,SELEX可以产生针对小的非约束性肽的高亲和力RNA配体。