Abstract

DNA is a compelling alternative to non-volatile information storage technologies due to its information density, stability, and energy efficiency. Previous studies have used artificially synthesized DNA to store data and automated next-generation sequencing to read it back. Here, we report digital Nucleic Acid Memory (dNAM) for applications that require a limited amount of data to have high information density, redundancy, and copy number. In dNAM, data is encoded by selecting combinations of single-stranded DNA with (1) or without (0) docking-site domains. When self-assembled with scaffold DNA, staple strands form DNA origami breadboards. Information encoded into the breadboards is read by monitoring the binding of fluorescent imager probes using DNA-PAINT super-resolution microscopy. To enhance data retention, a multi-layer error correction scheme that combines fountain and bi-level parity codes is used. As a prototype, fifteen origami encoded with ‘Data is in our DNA!\\n’ are analyzed. Each origami encodes unique data-droplet, index, orientation, and error-correction information. The error-correction algorithms fully recover the message when individual docking sites, or entire origami, are missing. Unlike other approaches to DNA-based data storage, reading dNAM does not require sequencing. As such, it offers an additional path to explore the advantages and disadvantages of DNA as an emerging memory material.

Highlights

  • DNA is a compelling alternative to non-volatile information storage technologies due to its information density, stability, and energy efficiency

  • By combining the spatial control of DNA nanotechnology with our error-correction algorithms, we demonstrate digital Nucleic Acid Memory (dNAM) as an alternative approach to prototyping DNA-based storage for applications that require a limited amount of data to have high information density, redundancy, and copy number

  • High-resolution atomic force microscopy (AFM) was used in tapping mode to confirm the structural integrity of the origami and the presence of the data domains (Fig. 1d). 40,000 frames from a single field of view were recorded using DNA-PAINT (~4500 origami identified in 2982 μm2)

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Summary

Introduction

DNA is a compelling alternative to non-volatile information storage technologies due to its information density, stability, and energy efficiency. In dNAM, data is encoded by selecting combinations of single-stranded DNA with (1) or without (0) docking-site domains. In dNAM, non-volatile information is digitally encoded into specific combinations of single-stranded. When formed into origami, the staple strands are arranged at addressable locations (Fig. 1) that define an indexed matrix of digital information. Extended staple strands have two domains: the first domain forms a sequence-specific double helix with the scaffold and determines the address of the data within the origami; the second domain extends above the origami and, if present, provides a docking site for fluorescently labeled single-stranded DNA imager strands. As an integrated memory platform, data is entered into dNAM when the staple strands encoding 1 or 0 are selected for each addressable site. The origami is optically imaged below the diffraction limit of light using DNA-PAINT (Fig. S1)

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