肽核酸序列选择性靶向双链DNA。

Peter E Nielsen
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引用次数: 0

摘要

序列选择性基因靶向是一种有吸引力的基因治疗药物发现方法,其目的是在转录水平上降低或增强特定基因的活性,或者作为靶向基因修复方法的一部分。伪多肽DNA模拟肽核酸(PNA)在三工、双工和双工侵入模式或非侵入三工模式下均能识别具有高序列特异性和亲和力的双工DNA。新的PNA修饰大大提高了通过双工入侵、双工入侵和三工识别DNA的亲和力。这种修饰也导致了靶向基因修复和基因组DNA序列选择性双链切割的新方法。
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Sequence-selective targeting of duplex DNA by peptide nucleic acids.

Sequence-selective gene targeting constitutes an attractive drug-discovery approach for genetic therapy, with the aim of reducing or enhancing the activity of specific genes at the transcriptional level, or as part of a methodology for targeted gene repair. The pseudopeptide DNA mimic peptide nucleic acid (PNA) can recognize duplex DNA with high sequence specificity and affinity in triplex, duplex and double-duplex invasive modes or non-invasive triplex modes. Novel PNA modification has improved the affinity for DNA recognition via duplex invasion, double-duplex invasion and triplex recognition considerably. Such modifications have also resulted in new approaches to targeted gene repair and sequence-selective double-strand cleavage of genomic DNA.

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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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