MnO2 nanosheet mediated "DD-A" FRET binary probes for sensitive detection of intracellular mRNA

被引:77
|
作者
Ou, Min [1 ]
Huang, Jin [1 ]
Yang, Xiaohai [1 ]
Quan, Ke [1 ]
Yang, Yanjing [1 ]
Xie, Nuli [1 ]
Wang, Kemin [1 ]
机构
[1] Hunan Univ, Key Lab Bionanotechnol & Mol Engn Hunan Prov, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
RESONANCE ENERGY-TRANSFER; NUCLEIC-ACID HYBRIDIZATION; BREAST-CANCER; THYMIDINE KINASE; FLUORESCENCE; NANOPROBE; PLATFORM; CELLS; DNA;
D O I
10.1039/c6sc03162e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The donor donor-acceptor (DD-A) FRET model has proven to have a higher FRET efficiency than donoracceptor acceptor (D-AA), donor-acceptor (D-A), and donor donor-acceptor acceptor (DD-AA) FRET models. The in-tube and in-cell experiments clearly demonstrate that the "DD-A"FRET binary probes can indeed increase the FRET efficiency and provide higher imaging contrast, which is about one order of magnitude higher than the ordinary "D-A"model. Furthermore, MnO2 nanosheets were employed to deliver these probes into living cells for intracellular TK1 mRNA detection because they can adsorb ssDNA probes, penetrate across the cell membrane and be reduced to Mn2+ ions by intracellular GSH. The results indicated that the MnO2 nanosheet mediated "DD-A"FRET binary probes are capable of sensitive and selective sensing gene expression and chemical-stimuli changes in gene expression levels in cancer cells. We believe that the MnO2 nanosheet mediated "DD-A"FRET binary probes have the potential as a simple but powerful tool for basic research and clinical diagnosis.
引用
收藏
页码:668 / 673
页数:6
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