Submicrometre geometrically encoded fluorescent barcodes self-assembled from DNA

被引:232
作者
Lin, Chenxiang [1 ,2 ,3 ]
Jungmann, Ralf [1 ,4 ]
Leifer, Andrew M. [5 ]
Li, Chao [1 ,6 ]
Levner, Daniel [1 ,6 ]
Church, George M. [1 ,6 ]
Shih, William M. [1 ,2 ,3 ]
Yin, Peng [1 ,4 ]
机构
[1] Harvard Univ, Wyss Inst Biologically Inspired Engn, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[5] Harvard Univ, Program Biophys, Cambridge, MA 02138 USA
[6] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
GENE-EXPRESSION; FOLDING DNA; ORIGAMI; PROTEINS; MICROSCOPY; TAG;
D O I
10.1038/NCHEM.1451
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The identification and differentiation of a large number of distinct molecular species with high temporal and spatial resolution is a major challenge in biomedical science. Fluorescence microscopy is a powerful tool, but its multiplexing ability is limited by the number of spectrally distinguishable fluorophores. Here, we used (deoxy) ribonucleic acid (DNA)-origami technology to construct submicrometre nanorods that act as fluorescent barcodes. We demonstrate that spatial control over the positioning of fluorophores on the surface of a stiff DNA nanorod can produce 216 distinct barcodes that can be decoded unambiguously using epifluorescence or total internal reflection fluorescence microscopy. Barcodes with higher spatial information density were demonstrated via the construction of super-resolution barcodes with features spaced by similar to 40 nm. One species of the barcodes was used to tag yeast surface receptors, which suggests their potential applications as in situ imaging probes for diverse biomolecular and cellular entities in their native environments.
引用
收藏
页码:832 / 839
页数:8
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