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A simple “turn-on” fluorescent biosensor for sensitive detection of exonuclease III activity through photoinduced electron transfer and self-hybridization of a DNA probe

机译:一个简单的“开启”荧光生物传感器,用于通过光诱导的电子转移和DNA探针的自杂交来灵敏地检测核酸外切酶III的活性

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Exonuclease III (Exo III) plays crucial roles in maintaining the genome stability. Herein, a turn-on fluorescence strategy for detection of Exo III activity is developed. In this strategy, a poly(CG) single-stranded DNA (ssDNA) probe is labeled with fluorescein amidite (FAM) at the 3′ end, and the ssDNA can self-hybridize to form double-stranded DNA (dsDNA). This dsDNA acts as the substrate for Exo III. Due to photoinduced electron transfer (PET) between FAM and guanine (G), the fluorescence of the FAM-labeled dsDNA probe is completely quenched. Upon the addition of Exo III, the dsDNA will be digested, and FAM emits very strong fluorescence. Thus, Exo III activity can be facilely measured with a simple fluorescence reader. This method has a wide detection range from 5 × 10?4 U mL?1 to 5 U mL?1 with a detection limit of 3 × 10?4 U mL?1. The results demonstrated herein may provide a new pattern for Exo III activity detection with high accuracy and good specificity as well as satisfactory applicability in real biosamples, which holds great potential for drug screening and basic research related to exonucleases.
机译:核酸外切酶III(Exo III)在维持基因组稳定性中起关键作用。本文中,开发了用于检测Exo III活性的开启荧光策略。在这种策略中,聚(CG)单链DNA(ssDNA)探针在3'端用荧光素酰胺(FAM)标记,并且ssDNA可以自杂交形成双链DNA(dsDNA)。该dsDNA充当Exo III的底物。由于FAM和鸟嘌呤(G)之间的光诱导电子转移(PET),FAM标记的dsDNA探针的荧光被完全淬灭。加入Exo III后,dsDNA将被消化,FAM发出非常强的荧光。因此,可以使用简单的荧光读取器轻松测量Exo III的活性。该方法的检测范围从5×10?4 U mL?1到5 U mL?1,检测限为3×10?4 U mL?1。本文证明的结果可为Exo III活性检测提供一种新模式,具有高精度,良好的特异性以及令人满意的在实际生物样品中的适用性,这为药物筛选和与核酸外切酶相关的基础研究具有巨大潜力。

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