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Thiazole orange-conjugated peptide nucleic acid for fluorescent detection of specific DNA sequences and site-selective photodamage

机译:噻唑橙缀合的肽核酸,用于特定DNA序列的荧光检测和位点选择性光损伤

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摘要

A fluorescent probe to detect specific sequences in double-stranded DNA (dsDNA) has been synthesized by conjugating thiazole orange (TO) with pseudo-complementary peptide nucleic acid (pcPNA). A pair of TO-conjugated pcPNAs bound to the target site in dsDNA through double-duplex invasion, and promoted intercalation of the TO moieties for notable enhancement of their fluorescence. Site-specificity of the detection is high enough to differentiate only one base-pair difference in DNA. These TO-pcPNA conjugates also function as site-selective photo-damage inducers. Upon irradiation with visible light, singlet oxygen was generated by energy transfer from the dyes at the invasion site, resulting in the site-selective formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxoG) there.
机译:通过将噻唑橙(TO)与伪互补肽核酸(pcPNA)缀合,可以合成检测双链DNA(dsDNA)中特定序列的荧光探针。一对TO-缀合的pcPNA通过双双链体入侵与dsDNA中的靶位点结合,并促进了TO部分的插入,从而显着增强了它们的荧光。检测的位点特异性很高,足以区分DNA中仅一个碱基对的差异。这些TO-pcPNA缀合物还用作位点选择性光损伤诱导剂。在可见光照射下,染料从入侵位点处的能量转移产生单线态氧,导致在那里选择性地形成8-oxo-7,8-dihydro-2'-deoxyguanosine(8-oxoG)。

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