In situ simultaneous monitoring of ATP and GTP using a graphene oxide nanosheet-based sensing platform in living cells

被引:206
作者
Wang, Ying [1 ]
Tang, Longhua [1 ]
Li, Zhaohui [2 ]
Lin, Yuehe [2 ,3 ]
Li, Jinghong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing Key Lab Microanalyt Methods & Instrumenta, Beijing 100084, Peoples R China
[2] Pacific NW Natl Lab, Richland, WA 99352 USA
[3] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
基金
中国国家自然科学基金;
关键词
AQUEOUS-SOLUTION; LABEL-FREE; APTAMERS; SENSOR; RECOGNITION; ADENOSINE; DESIGN;
D O I
10.1038/nprot.2014.126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we present a detailed protocol for in situ multiple fluorescence monitoring of adenosine-5'-triphosphate (ATPATPATP) and guanosine-5'-triphosphate (GTPTP) in MCF-7 breast cancer cells by using graphene oxide nanosheet (GO-nS) and DNANA/RNARNARNA aptamers. FAM-labeled ATPATPATP aptamer and Cy5-modified GTPTP aptamer are used to construct the multiple aptamer/GO-nS sensing platform through ` p-p stacking' between aptamers and GO-nS. Binding of aptamers to GO-nS guarantees the fluorescence resonance energy transfer between fluorophores and GO-nS, resulting in ` fluorescence off'. When the aptamer/GO-nS are transported inside the cells via endocytosis, the conformation of the aptamers will change on interaction with cellular ATPATPATP and GTPTP. On the basis of the fluorescence ` off/on' switching, simultaneous sensing and imaging of ATPATPATP and GTPTP in vitro and in situ have been realized through fluorescence and confocal microscopy techniques. In this protocol, we describe the synthesis of GO and GO-nS, preparation of aptamer/GO-nS platform, in vitro detection of ATPATPATP and GTPTP, and how to use this platform to realize intracellular ATPATPATP and GTPTP imaging in cultured MCF-7 cells. The preparation of GO-nS is anticipated to take 7-14 d, and assays involving microscopy imaging and MCF-7 cells culturing can be performed in 2-3 d.
引用
收藏
页码:1944 / 1955
页数:12
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