Lilley David M J
Cancer Research UK Nucleic Acid Structure Research Group, MSI/WTB Complex, The University of Dundee, Dundee, UK.
Biol Chem. 2007 Jul;388(7):699-704. doi: 10.1515/BC.2007.069.
A novel chemo-genetic approach for the analysis of general acid-base catalysis by nucleobases in ribozymes is reviewed. This involves substitution of a C-nucleoside with imidazole in place of a natural nucleobase. The Varkud satellite ribozyme in which the nucleobase at the critical 756 position has been replaced by imidazole is active in both cleavage and ligation reactions. Similarly, a modified hairpin ribozyme with the nucleobase at position 8 substituted by imidazole is active in cleavage and ligation reactions. Although the rates are lower than those of the natural ribozymes, they are significantly greater than other variants at these positions. The dependence of the hairpin ribozyme reaction rates on pH has been studied. Both cleavage and ligation reactions display a bell-shaped pH dependence, consistent with general acid-base catalysis involving the nucleotide at position 8.
综述了一种用于分析核酶中碱基通用酸碱催化作用的新型化学遗传学方法。这涉及用咪唑取代天然碱基来替换C - 核苷。关键756位碱基被咪唑取代的Varkud卫星核酶在切割和连接反应中均具有活性。同样,8位碱基被咪唑取代的修饰发夹核酶在切割和连接反应中也具有活性。尽管其反应速率低于天然核酶,但明显高于这些位置的其他变体。研究了发夹核酶反应速率对pH的依赖性。切割和连接反应均呈现钟形pH依赖性,这与涉及8位核苷酸的通用酸碱催化作用一致。