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Graphene Oxide-based Direct Measurement of DNase I Activity with Single Stranded DNA

机译:基于氧化石墨烯的单链DNA DNase I活性的直接测量

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摘要

Recent studies have shown that single-stranded DNA adsorbed onto graphene oxide is protected from DNase I cleavage. However, double-stranded DNA bound to graphene oxide and could be digested by DNase I. To elucidate whether single-stranded DNA is protect from DNase I in the presence of graphene oxide, this study conducted DNase I digestion using single-stranded DNA and single-stranded DNA containing the duplex region in the presence of graphene oxide. Addition of DNase I resulted in restoration of the fluorescence emission that had been quenched when DNA was adsorbed to graphene oxide. It indicates that DNase I cleaved the adsorbed single-stranded DNA onto graphene oxide, which was sufficient for the detection of DNase I activity.
机译:最近的研究表明,吸附在氧化石墨烯上的单链DNA受到DNase I切割的保护。但是,双链DNA结合到氧化石墨烯上,并可以被DNase I消化。为了阐明在存在氧化石墨烯的情况下单链DNA是否不受DNase I的影响,本研究使用单链DNA和单链DNA进行了DNase I消化。氧化石墨烯存在的含双链区的双链DNA。脱氧核糖核酸酶I的添加导致荧光发射的恢复,当DNA被吸附到氧化石墨烯上时,荧光发射被淬灭。这表明DNase I将吸附的单链DNA裂解到氧化石墨烯上,这足以检测DNase I的活性。

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