Cancer Research UK Nucleic Acid Structure Research Group, MSI/WTB Complex, The University of Dundee, Dundee DD15EH, United Kingdom.
RNA. 2011 Feb;17(2):213-21. doi: 10.1261/rna.2473711. Epub 2010 Dec 20.
The active centers of the hairpin and VS ribozymes are both generated by the interaction of two internal loops, and both ribozymes use guanine and adenine nucleobases to accelerate cleavage and ligation reactions. The centers are topologically equivalent and the relative positioning of key elements the same. There is good evidence that the cleavage reaction of the VS ribozyme is catalyzed by the guanine (G638) acting as general base and the adenine (A756) as general acid. We now critically evaluate the experimental mechanistic evidence for the hairpin ribozyme. We conclude that all the available data are fully consistent with a major contribution to catalysis by general acid-base catalysis involving the adenine (A38) and guanine (G8). It appears that the two ribozymes are mechanistically equivalent.
发夹状核酶和 VS 核酶的活性中心都是由两个内部环的相互作用产生的,两种核酶都使用鸟嘌呤和腺嘌呤核苷酸碱基来加速切割和连接反应。这些中心在拓扑上是等价的,关键元素的相对定位也是相同的。有充分的证据表明,VS 核酶的切割反应是由作为通用碱的鸟嘌呤(G638)和作为通用酸的腺嘌呤(A756)催化的。我们现在对发夹状核酶的实验机制证据进行了批判性评估。我们的结论是,所有可用的数据都完全一致,即通用酸碱催化对催化有重大贡献,涉及腺嘌呤(A38)和鸟嘌呤(G8)。这两种核酶在机制上似乎是等同的。