A cofactor mediated supramolecular oligo-adenine triplex for reprogrammable macroscopic hydrogel assembly

Alycia Zi Ting LIM, Michael Shao Min HO, Yujie KE, Wei Wei LOH, Zhaogang DONG, Fuke WANG, Jason Y.C. LIM, Xin Ting ZHENG, Le YANG, Yuwei HU*

*Corresponding author for this work

Research output: Journal PublicationsJournal Article (refereed)peer-review

Abstract

Noncanonical DNA structures mediated by low-molecular-weight cofactors significantly enrich the arsenal of the DNA toolbox and expand its functional applications. In this study, cyanuric acid (CA), a cofactor with three thymine-like edges, is employed to assemble adenine-rich strands (A-strands) into a parallel noncanonical A-CA triplex configuration through Watson-Crick and Hoogsteen interactions. This assembly occurs at a system pH value below the pKa of the CA cofactor (6.9), where CA is protonated, while its deprotonation at higher pH levels leads to the dissociation of the A-CA triplex into single A-strands and free CA cofactors. The structural transition is fully pH reversible. The A-CA triplex is further utilized as a crosslinking element for reprogrammable macroscopic object assembly, exemplified by hydrogel cubes (5 × 5 × 5 mm), a topic that has been less explored compared to nano- and microscopic constructs. Controlled, modular assembly and disassembly of various configurations, such as square, line, and T-shape, are demonstrated through reversible pH adjustments. This strategy offers a streamlined approach using a single DNA sequence and cofactor for hydrogel modification and complex construction, providing cost-effective, recyclable, and stimuli-responsive functionality, which inspires the development of versatile and adaptive supramolecular systems in chemistry and materials science.

Original languageEnglish
Pages (from-to)3393-3398
Number of pages6
JournalSoft Matter
Volume21
Issue number17
Early online date24 Mar 2025
DOIs
Publication statusPublished - 7 May 2025

Bibliographical note

Publisher Copyright:
© 2025 The Royal Society of Chemistry.

Funding

The research is supported by the Career Development Fund (C210112014), SERC Central Research Fund (CRF, UIBR, KIMR220901aSERCRF), and RIE2025 Manufacturing, Trade, and Connectivity (MTC) Programmatic Fund under grant M24M9b0013 entitled BLISS: Beyond Liquids with In-Situ Solid-state Surficial Sensorics, IMRE, A*STAR, Singapore. The kind assistance with the SEM by Karen Tang Yuanting is greatly appreciated.

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