Burke D H, Hoffman D C
Department of Molecular, Cellular, & Developmental Biology, Campus Box 347, University of Colorado, Boulder, Colorado 80309-0347, USA.
Biochemistry. 1998 Mar 31;37(13):4653-63. doi: 10.1021/bi972877p.
Specific recognition of nucleotide cofactors by RNA may be important in engineering new RNA enzymes (ribozymes). Although in vitro selections (SELEX) have identified nucleic acid motifs ("aptamers") that bind a variety of adenosine cofactors, none of these recognizes coenzyme A (CoA), the primary biological cofactor used in acyltransfer reactions. We used SELEX experiments with two random RNA pools to identify aptamers that bind CoA. Functional boundary determination and extensive comparative sequence analysis (including reselection of a mutagenized, circularly permuted RNA) led to the identification of a 52 nucleotide minimal aptamer ("min52"). The RNA structural motif contains a large internal loop with 26 unpaired nucleotides flanked by helices of any base-paired sequence. Twenty loop nucleotides are specifically required for binding activity, 12 of which are derived from the original primer binding sequences. Specificity studies with CoA analogues demonstrated that the aptamer recognizes many adenosine analogues, including ATP, and that recognition is predominantly through the Höogsteen face of adenine. Binding activity is greatest at acidic pH (optimum near 5.0), in low or no monovalent salt, and at high concentrations of either Mg2+ or Mn2+. Strong binding activity (86% of maximum) is observed at pH 4.0, suggesting that at least some extreme conditions (acidic pH) may be compatible with RNA World theories of the origin and early evolution of life. In the presence of 10 mM Mg2+, binding is unaffected by the addition of 1 mM Ca2+, but it is mildly inhibited by 1 mM Zn2+ or Co2+ or by 0.1 mM Cu2+ or Ni2+. The dissociation constant (Kd) for the association of min52 RNA with ATP in solution was measured to be 2.4 +/- 0.4 microM under the conditions of the selection and 0.5 +/- 0.1 microM under optimized conditions. Finally, we show that the selected CoA aptamer populations contain other RNAs at low frequencies that preferentially recognize intact CoA and are not eluted from the resin by AMP alone.
RNA对核苷酸辅因子的特异性识别在构建新型RNA酶(核酶)中可能很重要。尽管体外筛选(SELEX)已鉴定出能结合多种腺苷辅因子的核酸基序(“适体”),但这些都无法识别辅酶A(CoA),而CoA是酰基转移反应中使用的主要生物辅因子。我们使用两个随机RNA文库进行SELEX实验,以鉴定能结合CoA的适体。功能边界确定和广泛的比较序列分析(包括对诱变的、环状排列的RNA进行重新筛选)导致鉴定出一个52个核苷酸的最小适体(“min52”)。该RNA结构基序包含一个大的内部环,有26个未配对核苷酸,两侧是任意碱基配对序列的螺旋。结合活性特别需要20个环核苷酸,其中12个来自原始引物结合序列。对CoA类似物的特异性研究表明,该适体能识别许多腺苷类似物,包括ATP,且识别主要通过腺嘌呤的霍格思廷面。在酸性pH(最佳值接近5.0)、低或无单价盐以及高浓度的Mg2+或Mn2+条件下,结合活性最大。在pH 4.0时观察到强结合活性(为最大值的86%),这表明至少某些极端条件(酸性pH)可能与生命起源和早期进化的RNA世界理论相符。在存在10 mM Mg2+的情况下,添加1 mM Ca2+不影响结合,但添加1 mM Zn2+或Co2+或0.1 mM Cu2+或Ni2+会轻微抑制结合。在筛选条件下,min52 RNA与溶液中ATP结合的解离常数(Kd)经测定为2.4±0.4 μM,在优化条件下为0.5±0.1 μM。最后,我们表明所选的CoA适体群体中含有低频的其他RNA,它们优先识别完整的CoA,且不能仅通过AMP从树脂上洗脱下来。