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用于杂交分析的磷光寡核苷酸探针的合成与评估。

Synthesis and evaluation of phosphorescent oligonucleotide probes for hybridisation assays.

作者信息

O'Sullivan Paul J, Burke Martina, Soini Aleksi E, Papkovsky Dmitri B

机构信息

Biochemistry Department, University College Cork, Lee Maltings, Cork, Ireland.

出版信息

Nucleic Acids Res. 2002 Nov 1;30(21):e114. doi: 10.1093/nar/gnf113.

Abstract

Monofunctional, p-isothiocyanatophenyl-derivatives of platinum (II)-coproporphyrin-I (PtCP-NCS) were evaluated as phosphorescent labelling reagents for synthetic oligonucleotides containing a 3'- or 5'-amino modification. Synthesis and purification conditions were optimised to generate high yields and purity of PtCP-labelled oligonucleotide probes. Phosphorescent properties of the PtCP label have been shown to be largely unaffected by conjugation to oligonucleotides of various length, GC composition and label attachment site. 5'-PtCP-labelled oligonucleotides were shown to work efficiently as primers in a standard PCR. A dedicated 532 nm laser-based time-resolved fluorescence plate reader enabled highly sensitive detection of PtCP-labelled oligonucleotides and PCR products, both in solution and in agarose gels, with limits of detection in the order of 0.3 pM. A model system employing two complementary oligonucleotides labelled with PtCP and QSY 7 dye (dark quencher) showed strong (approximately 20-fold) and specific proximity quenching of PtCP label upon hybridisation in solution. The potential applications of PtCP-labelled probes in hybridisation assays were discussed.

摘要

对铂(II)-粪卟啉-I(PtCP-NCS)的单功能对异硫氰酸苯酯衍生物作为含3'-或5'-氨基修饰的合成寡核苷酸的磷光标记试剂进行了评估。优化了合成和纯化条件,以获得高产率和高纯度的PtCP标记寡核苷酸探针。已证明PtCP标记的磷光性质在很大程度上不受与各种长度、GC组成和标记连接位点的寡核苷酸偶联的影响。5'-PtCP标记的寡核苷酸在标准PCR中作为引物表现出高效性。一台专门的基于532nm激光的时间分辨荧光酶标仪能够在溶液和琼脂糖凝胶中对PtCP标记的寡核苷酸和PCR产物进行高灵敏度检测,检测限约为0.3pM。一个使用用PtCP和QSY 7染料(暗猝灭剂)标记的两条互补寡核苷酸的模型系统显示,在溶液中杂交时,PtCP标记有强烈(约20倍)且特异性的邻近猝灭。讨论了PtCP标记探针在杂交分析中的潜在应用。

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