DNA-Templated Assembly of a Heterobivalent Quantum Dot Nanoprobe For Extra- and Intracellular Dual-Targeting and Imaging of Live Cancer Cells

被引:79
作者
Wei, Wei [1 ]
He, Xuewen [1 ]
Ma, Nan [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Hlth Chem & Mol Diag Suzhou, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer; DNA; imaging agents; mRNA; quantum dots; RESONANCE ENERGY-TRANSFER; GENE DELIVERY; APTAMER; NANOCRYSTALS; LUMINESCENCE; SURVIVIN; AS1411;
D O I
10.1002/anie.201400428
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantum dots (QDs) hold great promise for the molecular imaging of cancer because of their superior optical properties. Although cell-surface biomarkers can be readily imaged with QDs, non-invasive live-cell imaging of critical intracellular cancer markers with QDs is a great challenge because of the difficulties in the automatic delivery of QD probes to the cytosol and the ambiguity of intracellular targeting signals. Herein, we report a new type of DNA-templated heterobivalent QD nanoprobes with the ability to target and image two spatially isolated cancer markers (nucleolin and mRNA) present on the cell surface and in the cell cytosol. Bypassing endolysosomal sequestration, this type of QD nanoprobes undergo macropinocytosis following the nucleolin targeting and then translocate to the cytosol for mRNA targeting. Fluorescence resonance energy transfer (FRET) based confocal microscopy enables unambiguous signal deconvolution of mRNA-targeted QD nanoprobes inside cancer cells.
引用
收藏
页码:5573 / 5577
页数:5
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