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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >In vitro selection of deoxyribozymes active with Cd2+ ions resulting in variants of DNAzyme 8-17
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In vitro selection of deoxyribozymes active with Cd2+ ions resulting in variants of DNAzyme 8-17

机译:体外选择具有Cd2 +离子活性的脱氧核酶,产生DNAzyme 8-17的变体

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In vitro selection was performed to search for RNA-cleaving DNAzymes catalytically active with Cd2+ ions from the oligonucleotide combinatorial library with a 23-nucleotide random region. All the selected, catalytically active variants turned out to belong to the 8-17 type DNAzyme. Three DNAzymes were prepared in shortened, cis-acting versions which were subjected to a detailed study of the kinetic properties and metal ion preferences. Although the selection protocol was designed for Cd2+-dependent DNAzymes, the variants showed broader metal ion specificity. They preferred Cd2+ but were also active with Mn2+ and Zn2+, suggesting that binding of the catalytic ion does not require an extremely specific coordination pattern. The unexpected decrease of the catalytic activity of the variants along with the temperature increase suggested that some changes occurred in their structures or the rate-limiting step of the reaction was changed. Two elements of the catalytic core of DNAzyme 1/VIIWS, the nucleotide at position 12 and the three-base-pair hairpin motif, were mutated. The presence of a purine residue at position 12 was crucial for the catalytic activity but the changes at that position had a relatively small influence on the metal ion preferences of this variant. The middle base pair of the three-base-pair hairpin was changed from A-T to C-G interaction. The catalytic activity of the mutated variant was increased with Zn2+, decreased with Mn2+, and was not changed in the presence of Cd2+ ions. Clearly, this base pair was important for defining the metal ion preferences of the DNAzyme 1/VIIWS.
机译:进行体外选择以从具有23个核苷酸随机区域的寡核苷酸组合文库中搜索具有Cd2 +离子催化活性的RNA切割DNA酶。所选择的所有催化活性变体均属于8-17型DNAzyme。制备了缩短的顺式作用形式的三种DNA酶,对它们进行了动力学性质和金属离子偏好的详细研究。尽管选择方案是针对Cd2 +依赖性DNA酶设计的,但这些变体显示出更广泛的金属离子特异性。他们更喜欢Cd2 +,但对Mn2 +和Zn2 +也有活性,表明催化离子的结合不需要非常特殊的配位模式。随着温度的升高,这些变体的催化活性出乎意料地降低,表明它们的结构发生了一些变化,或者反应的限速步骤发生了变化。 DNAzyme 1 / VIIWS催化核心的两个元素,第12位的核苷酸和三碱基对发夹基序被突变。位置12上嘌呤残基的存在对于催化活性至关重要,但该位置的变化对该变体的金属离子偏好性影响相对较小。三碱基对发夹的中间碱基对从A-T变为C-G相互作用。突变变体的催化活性随Zn2 +的增加而增加,随Mn2 +的下降而降低,并且在Cd2 +离子存在下不变。显然,该碱基对对于定义DNAzyme 1 / VIIWS的金属离子偏好至关重要。

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