Wang Dennis Y, Lai Beatrice H Y, Feldman Anat R, Sen Dipankar
Department of Molecular Biology and Biochemistry, Simon Fraser University, 8888 University Way, Burnaby, BC V5A 1S6, Canada.
Nucleic Acids Res. 2002 Apr 15;30(8):1735-42. doi: 10.1093/nar/30.8.1735.
A general approach is described for controlling the RNA-cleaving activity of nucleic acid enzymes (ribozymes and DNAzymes) via the use of oligonucleotide effectors (regulators). In contrast to the previously developed approaches of allosteric and facilitator-mediated regulation of such enzymes, this approach, called 'expansive' regulation, requires that the regulator bind simultaneously to both enzyme and substrate to form a branched three-way complex. Such three-way enzyme-substrate-regulator complexes are catalytically competent relative to the structurally unstable enzyme-substrate complexes. Using the 8-17 and bipartite DNAzymes and the hammerhead ribozyme as model systems, 20- to 30-fold rate enhancements were achieved in the presence of regulators of engineered variants of the above three enzymes, even under unoptimized conditions. Broadly, using this approach ribozyme and DNAzyme variants that are amenable to regulation by oligonucleotide effectors can be designed even in the absence of any knowledge of the folded structure of the relevant ribozyme or DNAzyme. Expansive regulation therefore represents a new and potentially useful technology for both the regulation of nucleic acid enzymes and the detection of specific RNA transcripts.
本文描述了一种通过使用寡核苷酸效应物(调节剂)来控制核酸酶(核酶和脱氧核酶)的RNA切割活性的通用方法。与先前开发的对这类酶进行变构调节和促进剂介导调节的方法不同,这种称为“扩展”调节的方法要求调节剂同时与酶和底物结合,形成一种分支的三向复合物。相对于结构不稳定的酶-底物复合物,这种三向酶-底物-调节剂复合物具有催化活性。以8-17和二分体脱氧核酶以及锤头状核酶作为模型系统,即使在未优化的条件下,在上述三种酶的工程变体的调节剂存在下,反应速率也提高了20至30倍。广泛地说,即使在对相关核酶或脱氧核酶的折叠结构一无所知的情况下,使用这种方法也可以设计出适合寡核苷酸效应物调节的核酶和脱氧核酶变体。因此,扩展调节对于核酸酶的调节和特定RNA转录本的检测而言,是一种新的且可能有用的技术。