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Updated: Oct 28, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
Published on: April 26, 2013
Beyond Static Architectures: Responsive Tetrahedral Framework Nucleic Acids for Precise Theranostics
Yang Gao1, Geru Zhang1, Xinyu Wu1
1State Key Laboratory of Oral Diseases, National Center for Stomatology, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan610041, China.
Abstract:
Precise theranostics requires spatiotemporal control and high specificity to adapt to complex physiological microenvironments. Tetrahedral framework nucleic acids (tFNA), classic 3D DNA nanostructures, offer distinct advantages such as atomic-level structural precision, intrinsic programmability, and excellent biocompatibility. While traditional static tFNA lack dynamic responsiveness to external stimuli─severely limiting their clinical translation potential─the emergence of dynamically responsive tFNA has garnered increasing attention. These smart systems offer substantial advantages, including stimulus-triggered structural reconfiguration, targeted payload release, and real-time signal transduction. Despite rapid design innovations, a systematic summary of dynamic tFNA strategies remains lacking. Accordingly, we synthesize the design principles of responsive tFNA by categorizing their mechanisms into conformational rearrangement, chemical bond cleavage, and toehold-mediated strand displacement logic. We highlight their applications in precision diagnosis, smart therapeutics, and theranostics integration and discuss critical challenges in biological stability, scalable manufacturing, and biosecurity. By mapping current advancements and unresolved hurdles, this work provides a comprehensive reference for the rational design of responsive DNA nanodevices and discusses the challenges associated with the clinical translation of dynamic tFNA.
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