DNA
核酸
荧光
生物物理学
化学
DNA纳米技术
材料科学
纳米技术
物理
组合化学
生物
生物化学
量子力学
作者
Dongfang Wang,Carolin Vietz,Tim Schröder,Guillermo P. Acuna,Birka Lalkens,Philip Tinnefeld
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-08-07
卷期号:17 (9): 5368-5374
被引量:101
标识
DOI:10.1021/acs.nanolett.7b01829
摘要
Sensing nucleic acids typically involves the recognition of a specific sequence and reporting by, for example, a fluorogenic reaction yielding one activated dye molecule per detected nucleic acid. Here, we show that after binding to a DNA origami track a bound DNA target (a "DNA walker") can release the fluorescence of many molecules by acting as the catalyst of an enzymatic nicking reaction. As the walking kinetics sensitively depends on the walker sequence, the resulting brightness distribution of DNA origamis is a sequence fingerprint with single-nucleotide sensitivity. Using Monte Carlo simulations, we rationalize that the random self-avoiding walk is mainly terminated when steps to nearest neighbors are exhausted. Finally, we demonstrate that the DNA walker is also active in a plasmonic hotspot for fluorescence enhancement, indicating the potential of combining different amplification mechanisms enabled by the modularity of DNA nanotechnology.
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