Facet-Based DNA Polyhedra for Lower-Complexity Assembly

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Solution Overview

Problem

Conventional DNA origami methods for constructing complex polyhedral structures are computationally intensive, require significant resources, and suffer from scalability issues due to reliance on a fixed-length scaffold and numerous staple strands, leading to high synthesis costs and structural instability.

Innovation Solution

A modular, bottom-up self-assembly method using single-stranded DNA oligonucleotides, each corresponding to a discrete face of the polyhedron, which self-assemble through localized hybridization without a scaffold or staples, facilitated by edge-specific hybridization domains and enhanced by surface acoustic waves for spatial clustering.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional DNA origami methods are used to construct complex polyhedral structures, then geometric precision and structural complexity can be achieved, but computational resources and synthesis costs increase significantly

Engineering Contradiction:
Improvegeometric precisionVSAvoidcomputational complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent divides the DNA polyhedron construction into discrete modular units (oligonucleotides) that correspond to individual faces or edges of the polyhedron. Each oligonucleotide is designed with specific hybridization domains that enable self-assembly into the target geometric structure, eliminating the need for complex computational routing of long scaffold strands through hundreds of staple strands.

Inventive Principle:
Principle #1Segmentation

2Stability of the object's composition

If scaffold-based DNA origami methods are used, then structured assembly can be achieved, but scalability and adaptability are limited due to fixed-length scaffold requirements

Engineering Contradiction:
Improvestructural stabilityVSAvoidshape modularity
Core Design Contradiction:
Stability of the object's compositionVSAdaptability or versatility

Solution Approach 1:

The patent employs dynamic, adaptable oligonucleotide sequences that can be reconfigured to form different polyhedral structures. The modular design allows the same basic building blocks to be rearranged into various geometric configurations ( Platonic solids, Archimedean solids, etc.) by changing the hybridization patterns, enabling both structural stability and shape versatility without fixed scaffold constraints.

Inventive Principle:
Principle #15Dynamics

3Manufacturing precision

If numerous staple strands are used in DNA origami, then precise folding can be achieved, but purification complexity and robustness in low-concentration systems deteriorate

Engineering Contradiction:
Improvefolding precisionVSAvoidpurification ease
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The patent merges the functions of multiple staple strands into fewer, longer oligonucleotides that can perform multiple hybridization tasks simultaneously. This consolidation reduces the total number of distinct components required, simplifying purification procedures and improving system robustness in low-concentration conditions while maintaining the precision needed for accurate polyhedral formation.

Inventive Principle:
Principle #5Merging (Combining)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables efficient, scalable, and stable construction of DNA polyhedra with high fidelity, suitable for nanoelectronics and sensing applications, demonstrating enhanced structural integrity and thermal stability up to 84.5°C, with applications in targeted drug delivery and diagnostics.

Implementation Method 1

Each ssDNA oligonucleotide includes one or more edge-specific hybridization domains, designed to selectively hybridize with complementary domains on ssDNA strands defining adjacent faces.

Methodology Applied
Scientific EffectHybridization: Chemical Bonding

Implementation Method 2

facilitated by edge-specific hybridization domains and enhanced by surface acoustic waves for spatial clustering.

Methodology Applied
Scientific EffectSurface acoustic waves: Surface Acoustic Wave

Implementation Method 3

annealing the assembly mixture in a thermal cycler by incubating at 95° C. for 2 to 5 minutes then slowly annealed from 95° C. to 20° C. at the rate of 4 to 5° C./hour

Methodology Applied
Scientific EffectAnnealing: Annealing

Data Source

PatentUS20250332282A1Facet-based nucleic acid platonic, kepler-poinsot polyhedra and four-dimensional tesseract for therapeutic, diagnostic and analytical applications
Publication Date: 2025.10.30 THE UNIVERSITY OF HONG KONG
  • US20250332282A1 patent drawing
  • US20250332282A1 patent drawing
  • US20250332282A1 patent drawing

AI summary

Facet-based DNA polyhedral nanostructures with single strands of DNA for each polyhedron face. The DNA-based polyhedral nanostructures may be configured for targeted drug delivery and cell imaging for therapeutic, diagnostic and analytical diagnostic applications. The DNA polyhedral nanostructures adopt platonic icosahedral and dodecahedral configurations resembling the natural shapes of viral nucleocapsid proteins. The DNA polyhedral nanostructures address multiple technical challenges in the biomedical and biotechnological fields, including reducing the cost and complexity associated with conventional DNA origami systems, enhancing the sensitivity of diagnostic platforms, improving tracer delivery and signal clarity in PET and MRI, providing structural stability for nanostructure and payload integrity, and improving the resolution of Cryo-EM imaging of small molecules.