Issue 24, 2021

Fast-responding functional DNA superstructures for stimuli-triggered protein release

Abstract

Strategies that speed up the on-command release of proteins (e.g., enzymes) from stimuli-responsive materials are intrinsically necessary for biosensing applications, such as point-of-care testing, as they will achieve fast readouts with catalytic signal-amplification. However, current systems are challenging to work with because they usually exhibit response times on the order of hours up to days. Herein, we report on the first effort to construct a fast-responding gating system using protein-encapsulating functional DNA superstructures (denoted as protein@3D DNA). Proteins were directly embedded into 3D DNA during the one-pot rolling circle amplification process. We found that the specific DNA–DNA interaction and aptamer–ligand interaction could act as general protocols to release the loaded proteins from 3D DNA. The resulting gating system exhibits fast release kinetics on the order of minutes. Taking advantage of this finding, we designed a simple paper device by employing protein@3D DNA for colorimetric detection of toxin B (Clostridium difficile marker). This device is capable of detecting 0.1 nM toxin B within 16 minutes.

Graphical abstract: Fast-responding functional DNA superstructures for stimuli-triggered protein release

Supplementary files

Article information

Article type
Edge Article
Submitted
09 Feb 2021
Accepted
06 May 2021
First published
07 May 2021
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2021,12, 8282-8287

Fast-responding functional DNA superstructures for stimuli-triggered protein release

Y. Zhang, Q. Zhang, F. Cheng, Y. Chang, M. Liu and Y. Li, Chem. Sci., 2021, 12, 8282 DOI: 10.1039/D1SC00795E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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