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A general purpose RNA-cleaving DNA enzyme

机译:通用的RNA切割DNA酶

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摘要

An in vitro selection procedure was used to develop a DNA enzyme that can be made to cleave almost any targeted RNA substrate under simulated physiological con- ditions. The enzyme is comprised of a catalytic domain of 15 deoxynucleotides, flanked by two substrate-recognition do- mains of seven to eight deoxynucleotides each. The RNA substrate is bound through Watson-Crick base pairing and is cleaved at a particular phosphodiester located between an unpaired purine and a paired pyrimidine residue.
机译:使用体外选择程序开发了一种DNA酶,该酶可以在模拟的生理条件下裂解几乎所有靶向的RNA底物。该酶由15个脱氧核苷酸的催化结构域组成,两侧是两个底物识别域,每个域有7至8个脱氧核苷酸。 RNA底物通过沃森-克里克碱基配对结合,并在未配对的嘌呤和配对的嘧啶残基之间的特定磷酸二酯处裂解。

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