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      Photon-directed multiplexed enzymatic DNA synthesis for molecular digital data storage

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          Abstract

          New storage technologies are needed to keep up with the global demands of data generation. DNA is an ideal storage medium due to its stability, information density and ease-of-readout with advanced sequencing techniques. However, progress in writing DNA is stifled by the continued reliance on chemical synthesis methods. The enzymatic synthesis of DNA is a promising alternative, but thus far has not been well demonstrated in a parallelized manner. Here, we report a multiplexed enzymatic DNA synthesis method using maskless photolithography. Rapid uncaging of Co 2+ ions by patterned UV light activates Terminal deoxynucleotidyl Transferase (TdT) for spatially-selective synthesis on an array surface. Spontaneous quenching of reactions by the diffusion of excess caging molecules confines synthesis to light patterns and controls the extension length. We show that our multiplexed synthesis method can be used to store digital data by encoding 12 unique DNA oligonucleotide sequences with video game music, which is equivalent to 84 trits or 110 bits of data.

          Abstract

          Writing data in DNA is still a bottleneck due to the reliance on chemical synthesis methods. Here the authors report multiplexed enzymatic DNA synthesis using maskless photolithography.

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          Most cited references23

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          Next-generation digital information storage in DNA.

          Digital information is accumulating at an astounding rate, straining our ability to store and archive it. DNA is among the most dense and stable information media known. The development of new technologies in both DNA synthesis and sequencing make DNA an increasingly feasible digital storage medium. We developed a strategy to encode arbitrary digital information in DNA, wrote a 5.27-megabit book using DNA microchips, and read the book by using next-generation DNA sequencing.
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            Large-scale de novo DNA synthesis: technologies and applications

            This Review discusses large-scale de novo DNA synthesis via oligos or arrays, describes gene assembly and error correction and considers applications for large-scale DNA synthesis.
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              Towards practical, high-capacity, low-maintenance information storage in synthesized DNA.

              Digital production, transmission and storage have revolutionized how we access and use information but have also made archiving an increasingly complex task that requires active, continuing maintenance of digital media. This challenge has focused some interest on DNA as an attractive target for information storage because of its capacity for high-density information encoding, longevity under easily achieved conditions and proven track record as an information bearer. Previous DNA-based information storage approaches have encoded only trivial amounts of information or were not amenable to scaling-up, and used no robust error-correction and lacked examination of their cost-efficiency for large-scale information archival. Here we describe a scalable method that can reliably store more information than has been handled before. We encoded computer files totalling 739 kilobytes of hard-disk storage and with an estimated Shannon information of 5.2 × 10(6) bits into a DNA code, synthesized this DNA, sequenced it and reconstructed the original files with 100% accuracy. Theoretical analysis indicates that our DNA-based storage scheme could be scaled far beyond current global information volumes and offers a realistic technology for large-scale, long-term and infrequently accessed digital archiving. In fact, current trends in technological advances are reducing DNA synthesis costs at a pace that should make our scheme cost-effective for sub-50-year archiving within a decade.
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                Author and article information

                Contributors
                richie.kohman@wyss.harvard.edu
                gchurch@genetics.med.harvard.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                16 October 2020
                16 October 2020
                2020
                : 11
                : 5246
                Affiliations
                [1 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Genetics, , Harvard Medical School, ; Boston, MA 02115 USA
                [2 ]GRID grid.38142.3c, ISNI 000000041936754X, Wyss Institute for Biologically Inspired Engineering, ; Boston, MA 02115 USA
                [3 ]GRID grid.116068.8, ISNI 0000 0001 2341 2786, MIT Media Lab, , Massachusetts Institute of Technology, ; Cambridge, MA 02139 USA
                [4 ]GRID grid.417533.7, ISNI 0000 0004 0634 6125, Charles Stark Draper Laboratory, ; Cambridge, MA 02139 USA
                [5 ]GRID grid.222754.4, ISNI 0000 0001 0840 2678, Department of Biomedical Engineering, , Korea University, ; 466 Hana Science Hall, 145 Anamro, Seongbukgu, 02841 Seoul, South Korea
                Author information
                http://orcid.org/0000-0001-8299-5125
                http://orcid.org/0000-0001-6878-9990
                http://orcid.org/0000-0003-3535-2076
                Article
                18681
                10.1038/s41467-020-18681-5
                7567835
                33067441
                961826a9-ae43-4c63-a015-5fbc348f98fb
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 March 2020
                : 27 August 2020
                Categories
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                Custom metadata
                © The Author(s) 2020

                Uncategorized
                dna sequencing,dna and rna,synthetic biology
                Uncategorized
                dna sequencing, dna and rna, synthetic biology

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