2022
DOI: 10.1039/d1an02273c
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DNA tile self-assembly driven by antibody-mediated four-way branch migration

Abstract: With the rapid development of DNA nanotechnology, the reasonable construction and precise control of complex DNA nanostructures have become active research areas. The effective combination of proteins and other biomacromolecules...

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Cited by 2 publications
(2 citation statements)
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“…In the future design, we will continue our research based on the reusability and parallel information processing capability of self-resetting DNA switching circuits to explore multi-signal detection technologies in actual biological samples. In addition, we will further combine the selective function of self-resetting DNA switches with selfassembled structures 47,48 and macromolecular proteins such as antibodies 49,50 to provide programmable tools for building intelligent nanomachines, highly specific drug delivery systems, and multi-signal detection and reusable biosensors.…”
Section: Discussionmentioning
confidence: 99%
“…In the future design, we will continue our research based on the reusability and parallel information processing capability of self-resetting DNA switching circuits to explore multi-signal detection technologies in actual biological samples. In addition, we will further combine the selective function of self-resetting DNA switches with selfassembled structures 47,48 and macromolecular proteins such as antibodies 49,50 to provide programmable tools for building intelligent nanomachines, highly specific drug delivery systems, and multi-signal detection and reusable biosensors.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, more reliable ways can be explored to reduce the crosstalk between the biochemical signals, such as antibody-mediated DNA strand displacement, rather than only single-stranded DNA molecules for signal transduction. In future work, this programmable DNA finite-state machine with the sequential input of response time will be further studied to assist and control the self-assembly of complex structures [ 51 ], which will provide vital programmable control tools for building complex molecular machines. It is also possible to configure suitable binding sequences to design the activator as aptamers [ 52 ] or other biological signals [ 53 ] for the control of temporal information such as drug release.…”
Section: Discussionmentioning
confidence: 99%