DNA Data Storage Electrode Array for Scalable Polynucleotide Synthesis

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing biomolecule-based information storage systems lack scalability, automation, and efficiency for generating biomolecules, necessitating a need for larger capacity and more stable storage solutions.

Innovation Solution

The development of devices and methods utilizing a solid support with addressable loci and electrodes for polynucleotide synthesis, enabling high-density polynucleotide storage and synthesis through localized electrochemical control and digital fluidics, reducing cycle times and reagent usage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If traditional biomolecule-based information storage systems are used, then storage capacity is limited, but increasing storage capacity requires more complex and less scalable systems

Engineering Contradiction:
Improvestorage capacityVSAvoidsystem complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The system divides the storage surface into discrete addressable loci (e.g., 100 x 100 micrometer squares) that can be independently addressed and controlled. Each locus can hold polynucleotides, and the grid structure enables scalable expansion without increasing overall system complexity. This segmentation allows the system to achieve high storage capacity while maintaining manageable complexity through modular addressing.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent transitions from linear or simple 2D storage arrangements to a structured 2D grid system with precise addressing capabilities. By organizing loci in a dimensional grid (e.g., 1000 x 1000 addressable locations), the system exponentially increases storage capacity while maintaining systematic control. This dimensional organization enables scalable expansion by simply adding more grid positions rather than complicating the control architecture.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Productivity

If manual or less automated methods are used for polynucleotide synthesis, then system simplicity is maintained, but productivity and synthesis efficiency are low

Engineering Contradiction:
Improvesynthesis efficiencyVSAvoidautomation level
Core Design Contradiction:
ProductivityVSExtent of automation

Solution Approach 1:

The system employs electrochemical generation of reagents directly at the addressable loci, where electrical potentials applied to electrodes locally generate cleavage and deprotection reagents on-demand. This eliminates the need for complex automated reagent delivery systems while maintaining high productivity. The synthesis process serves itself by using electricity (a simple utility) to generate the necessary chemical reagents at the point of use, dramatically simplifying automation requirements.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent replaces mechanical reagent delivery systems (pumps, valves, fluid handling) with electrochemical generation at the locus level. Instead of mechanically transporting reagents to each location, the system uses electrical potentials to generate reagents in-situ through electrochemical reactions. This substitution dramatically reduces the complexity of automated fluid handling while maintaining high synthesis productivity and precision.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Loss of substance

If conventional synthesis methods are used, then reagent usage is high, but reducing reagent usage requires more precise localized control

Engineering Contradiction:
Improvereagent usageVSAvoidlocalized control precision
Core Design Contradiction:
Loss of substanceVSManufacturing precision

Solution Approach 1:

The system applies electrical potentials to specific electrodes corresponding to individual addressable loci, generating reagents only where needed. Each locus receives reagents locally through electrochemical generation at its specific position, rather than flooding the entire surface. This localized reagent generation dramatically reduces overall reagent consumption while requiring precise control of electrical potentials at each electrode location, which is achieved through the addressable electrode array.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The electrodes serve as intermediaries between the electrical control system and the chemical synthesis process. Electrical potentials applied to electrodes generate reagents in-situ at each addressable locus through electrochemical reactions. This intermediary mechanism enables precise localized reagent generation without requiring complex fluid delivery systems, reducing reagent waste while maintaining the precision needed for selective polynucleotide synthesis at specific loci.

Inventive Principle:
Principle #24Intermediary (Mediator)

4Productivity

If longer synthesis cycles are used, then manufacturing precision can be maintained, but productivity and throughput decrease

Engineering Contradiction:
Improvesynthesis throughputVSAvoidsynthesis accuracy
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The system enables continuous synthesis operations by rapidly cycling through the steps of nucleoside coupling, cleavage, and deprotection at each addressable locus. Electrical potentials are applied in rapid succession to generate reagents and drive reactions without long idle periods. The electrochemical generation of reagents on-demand eliminates waiting times for reagent delivery and preparation, maintaining continuous productive action while ensuring each synthesis step completes with sufficient precision through controlled potential application.

Inventive Principle:
Principle #20Continuity of useful action

Solution Approach 2:

The synthesis process uses periodic application of electrical potentials to drive sequential reactions at each locus. Electrical pulses are applied in a repeating cycle: coupling potential, cleavage potential, deprotection potential, then repeat for the next nucleoside. This periodic electrochemical driving enables rapid cycling through synthesis steps, increasing throughput while maintaining precision through controlled pulse timing and potential magnitudes that ensure complete reaction at each stage.

Inventive Principle:
Principle #19Periodic action

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

This approach enhances storage capacity and efficiency by allowing for higher polynucleotide densities and reduced synthesis times, providing a stable and scalable solution for biomolecule-based information storage.

Implementation Method 1

The bottom electrode is in addressable communication with the synthesis surface

Methodology Applied
Scientific EffectElectrochemical reaction: Electrolysis

Implementation Method 2

the at least one sidewall electrode is 50 nm to 200 nm from the bottom region

Methodology Applied
Scientific EffectElectrochemical reaction: Electrolysis

Data Source

PatentEP4715681A2DNA-based digital information storage
Publication Date: 2026.03.25 ATLAS DATA STORAGE INC
  • EP4715681A2 patent drawingFigure 1
  • EP4715681A2 patent drawingFigure 2
  • EP4715681A2 patent drawingFigure 3

AI summary

Provided herein are compositions, devices, systems and methods for generation and use of biomolecule-based information for storage. Further provided are devices comprising addressable electrodes controlling polynucleotide synthesis (deprotection, extension, or cleavage, etc.) The compositions, devices, systems and methods described herein provide improved storage, density, and retrieval of biomolecule-based information.