4.8 Article

Photoactivated DNA Walker Based on DNA Nanoflares for Signal-Amplified MicroRNA Imaging in Single Living Cells

Journal

ANALYTICAL CHEMISTRY
Volume 93, Issue 48, Pages 16264-16272

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c04505

Keywords

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Funding

  1. National Natural Science Foundation of China [21974127, 22090050, 21874121]
  2. National Key Research and Development Program of China [2018YFE0206900]
  3. Hubei Provincial Natural Science Foundation of China [2020CFA037]
  4. Zhejiang Provincial Natural Science Foundation of China [LD21B050001, LY20B050001]

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A photoactivated DNA walker signal amplification strategy was developed for photocontrollable imaging of cancer-related miRNA in single living cells. The method allows on-demand activation of the DNA walker for specified signal amplification imaging of cancer-related miRNA.
Specific and sensitive detection and imaging of cancer-related miRNA in living cells are desirable for cancer diagnosis and treatment. Because of the spatiotemporal variability of miRNA expression level during different cell cycles, signal amplification strategies that can be activated by external stimuli are required to image miRNAs on demand at desired times and selected locations. Herein, we develop a signal amplification strategy termed as the photoactivated DNA walker based on DNA nanoflares, which enables photocontrollable signal amplification imaging of cancer-related miRNA in single living cells. The developed method is achieved via combining photoactivated nucleic acid displacement reaction with the traditional exonuclease III (EXO III)-assisted DNA walker based on DNA nanoflares. This method is capable of on-demand activation of the DNA walker for dictated signal amplification imaging of cancer-related miRNA in single living cells. The developed method was demonstrated as a proof of concept to achieve photoactivated signal amplification imaging of miRNA-21 in single living HeLa cells via selective two-photon irradiation (lambda = 740 nm) of single living HeLa cells by using confocal microscopy equipped with a femtosecond laser.

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