A label-free fluorescent assay for deoxyribonuclease I activity based on DNA-templated silver nanocluster/graphene oxide nanocomposite

被引:43
|
作者
Lee, Chang Yeol [1 ]
Park, Ki Soo [1 ]
Jung, Yun Kyung [2 ]
Park, Hyuri Gyu [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, BK Program 21, Daehak Ro 291, Taejon 305701, South Korea
[2] UNIST, Dept Energy & Chem Engn, UNIST Gil 50, Ulsan 689798, South Korea
来源
基金
新加坡国家研究基金会;
关键词
Deoxyribonuclease I; RNA/DNA hybrid; DNA-templated silver nanocluster; Graphene oxide; Nanocomposite; Fluorescent enzyme assay; TRANSIENT MYOCARDIAL-ISCHEMIA; GRAPHENE OXIDE; AG NANOCLUSTERS; SERUM; BIOSENSOR; MARKER;
D O I
10.1016/j.bios.2016.08.073
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel label-free system for the sensitive fluorescent detection of deoxyribonuclease I (DNase I) activity has been developed by utilizing DNA-templated silver nanocluster/graphene oxide (DNA-AgNC/GO) nanocomposite. AgNC is first synthesized around C-rich template DNA and the resulting DNA-AgNC binds to GO through the interaction between the extension DNA and GO. The resulting DNA-AgNC/GO would show quite reduced fluorescence signal because the fluorescence from DNA-AgNCs is quenched by GO. In the presence of DNase I, however, it degrades the DNA strand within DNA/RNA hybrid duplex probe employed in this study, consequently releasing RNA which is complementary to the extension DNA. The released free RNA then extracts DNA-AgNC from GO by hybridizing with the extension DNA bound to GO. This process would restore the quenched fluorescence, emitting highly enhanced fluorescence signal. By employing this assay principle, DNase I activity was reliably identified with a detection limit of 0.10 U/ml which is lower than those from previous fluorescence-based methods. Finally, the practical capability of this assay system was successfully demonstrated by its use to determine DNase I activity in bovine urine. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 297
页数:5
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