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Pseudocomplementary PNAs as selective modifiers of protein activity on duplex DNA: the case of type IIs restriction enzymes

机译:伪互补PNA作为双链DNA上蛋白质活性的选择性修饰剂:II型限制酶的情况

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摘要

This study evaluates the potential of pseudocomplementary peptide nucleic acids (pcPNAs) for sequence-specific modification of enzyme activity towards double-stranded DNA (dsDNA). To this end, we analyze the ability of pcPNA-dsDNA complexes to site-selectively interfere with the action of four type IIs restriction enzymes. We have found that pcPNA-dsDNA complexes exhibit a different degree of DNA protection against cleavingicking activity of various isoschizomeric endonucleases under investigation (Plel, Mlyl and N. BstNBI) depending on their type and mutual arrangement of PNA-binding and enzyme recognition/cleavage sites. We have also found that the pcPNA targeting to closely located Plele or Bbsl recognition sites on dsDNA generates in some cases the nicking activity of these DNA cutters. At the same time, Mlyl endonuclease, a Plel isoschizomer, does not exhibit any DNA nicking/cleavage activity, being completely blocked by the nearby pcPNA binding. Our results have general implications for effective pc PNA interference with the performance of DNA-processing proteins, thus being important for prospecive applications of pcPNAs.
机译:这项研究评估了伪互补肽核酸(pcPNAs)对双链DNA(dsDNA)的酶活性进行序列特异性修饰的潜力。为此,我们分析了pcPNA-dsDNA复合物的位点选择性干扰四种IIs型限制酶作用的能力。我们发现,pcPNA-dsDNA复合物对被研究的各种同工质内切核酸酶(Plel,Mlyl和N. BstNBI)的裂解/切口活性表现出不同程度的DNA保护,这取决于它们的类型以及PNA结合和酶识别/裂解位点。我们还发现,在某些情况下,靶向于dsDNA上紧邻的Plele或Bbs1识别位点的pcPNA会产生这些DNA切割剂的切刻活性。同时,Mlyl核酸内切酶(一种Plel异构体)不表现出任何DNA切刻/切割活性,被附近的pcPNA结合完全阻断。我们的研究结果对有效pc PNA干扰DNA加工蛋白的性能具有一般意义,因此对于pcPNA的预期应用非常重要。

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