Burgin A B, Gonzalez C, Matulic-Adamic J, Karpeisky A M, Usman N, McSwiggen J A, Beigelman L
Ribozyme Pharmaceuticals Inc., Boulder, Colorado 80301, USA.
Biochemistry. 1996 Nov 12;35(45):14090-7. doi: 10.1021/bi961264u.
A site-specific chemical modification strategy has been employed to elucidate structure-function relationships at the only phylogenetically nonconserved position within the core of the hammerhead ribozyme (N7). Four different base substitutions at position 7 resulted in increased catalytic rates. A pyridin-4-one base substitution increased the rate of the chemical step up to 12-fold. These results are the first examples of chemical modifications within a catalytic RNA that enhance the rate of the chemical step. Four base substitutions resulted in decreased catalytic rates. The results do not correlate with proposed hydrogen bond interactions (Pley et al., 1994; Scott et al., 1995). This study demonstrates the utility of using unnatural nucleotide analogs-rather than mutagenesis with the four standard nucleotides alone-to elucidate structure-function relationships of small RNAs.
已采用位点特异性化学修饰策略来阐明锤头状核酶核心区域内唯一系统发育上不保守的位置(N7)的结构-功能关系。7位的四种不同碱基取代导致催化速率增加。吡啶-4-酮碱基取代使化学步骤的速率提高了12倍。这些结果是催化性RNA中增强化学步骤速率的化学修饰的首个实例。四种碱基取代导致催化速率降低。这些结果与所提出的氢键相互作用不相关(Pley等人,1994年;Scott等人,1995年)。本研究证明了使用非天然核苷酸类似物而非仅用四种标准核苷酸进行诱变来阐明小RNA结构-功能关系的实用性。