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Stimuli-Responsive DNA Nanomachines for Intracellular Targeted Electrochemiluminescence Imaging in Single Cells. | LitMetric

AI Article Synopsis

  • Electrochemiluminescence (ECL) microscopy is a powerful imaging technique for single cells that currently faces challenges in controlled intracellular imaging.
  • Researchers developed a DNA nanomachine that responds to stimuli to allow for ECL imaging of specific biomolecules inside single cells, using an innovative structure that activates upon the presence of ATP.
  • This new method not only enables targeted imaging of ATP distribution but can also be adapted for imaging other biomolecules by altering the DNA sequence, potentially enhancing ECL applications in cellular studies.

Article Abstract

Electrochemiluminescence (ECL) microscopy has emerged as a powerful technique for single-cell imaging owing to its unparalleled background-free imaging advantages. However, controlled intracellular ECL imaging remains challenging. Here, we developed a stimuli-responsive self-assembled DNA nanomachine that enables the ECL imaging of intracellular target biomolecules in single cells. The ECL nanoprobe consists of an ECL nanoemitter constructed from Ru(bpy)32+-doped metal-organic framework as the nanoreactor core, with a DNA polymer hydrogel shell (DNAgel) acting as the stimuli-gated layer. The outer functionalized DNAgel of the ECL nanoprobe was specifically designed to block ECL generation and to dissociate by ATP molecules, thereby enabling selective recovery of ECL emission capability. Such an engineered stimuli-responsive nanomachine successfully achieved the targeted ECL imaging of intracellular ATP distribution with spatial resolution. In addition, ECL imaging of various intracellular biomolecules should be generalizable by simply changing the switching DNA sequence of the probe. Our research provided a reliable strategy for ECL microscopy within cells, which will broaden the application of ECL in single-cell and single-molecule profiling.

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Source
http://dx.doi.org/10.1002/anie.202421658DOI Listing

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