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Information decay and enzymatic information recovery for DNA data storage
Synthetic DNA has been proposed as a storage medium for digital information due to its high theoretical storage density and anticipated long storage horizons. However, under all ambient storage conditions, DNA undergoes a slow chemical decay process resulting in nicked (broken) DNA strands, and the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584896/ https://www.ncbi.nlm.nih.gov/pubmed/36266439 http://dx.doi.org/10.1038/s42003-022-04062-9 |
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author | Meiser, Linda C. Gimpel, Andreas L. Deshpande, Tejas Libort, Gabriela Chen, Weida D. Heckel, Reinhard Nguyen, Bichlien H. Strauss, Karin Stark, Wendelin J. Grass, Robert N. |
author_facet | Meiser, Linda C. Gimpel, Andreas L. Deshpande, Tejas Libort, Gabriela Chen, Weida D. Heckel, Reinhard Nguyen, Bichlien H. Strauss, Karin Stark, Wendelin J. Grass, Robert N. |
author_sort | Meiser, Linda C. |
collection | PubMed |
description | Synthetic DNA has been proposed as a storage medium for digital information due to its high theoretical storage density and anticipated long storage horizons. However, under all ambient storage conditions, DNA undergoes a slow chemical decay process resulting in nicked (broken) DNA strands, and the information stored in these strands is no longer readable. In this work we design an enzymatic repair procedure, which is applicable to the DNA pool prior to readout and can partially reverse the damage. Through a chemical understanding of the decay process, an overhang at the 3’ end of the damaged site is identified as obstructive to repair via the base excision-repair (BER) mechanism. The obstruction can be removed via the enzyme apurinic/apyrimidinic endonuclease I (APE1), thereby enabling repair of hydrolytically damaged DNA via Bst polymerase and Taq ligase. Simulations of damage and repair reveal the benefit of the enzymatic repair step for DNA data storage, especially when data is stored in DNA at high storage densities (=low physical redundancy) and for long time durations. |
format | Online Article Text |
id | pubmed-9584896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95848962022-10-22 Information decay and enzymatic information recovery for DNA data storage Meiser, Linda C. Gimpel, Andreas L. Deshpande, Tejas Libort, Gabriela Chen, Weida D. Heckel, Reinhard Nguyen, Bichlien H. Strauss, Karin Stark, Wendelin J. Grass, Robert N. Commun Biol Article Synthetic DNA has been proposed as a storage medium for digital information due to its high theoretical storage density and anticipated long storage horizons. However, under all ambient storage conditions, DNA undergoes a slow chemical decay process resulting in nicked (broken) DNA strands, and the information stored in these strands is no longer readable. In this work we design an enzymatic repair procedure, which is applicable to the DNA pool prior to readout and can partially reverse the damage. Through a chemical understanding of the decay process, an overhang at the 3’ end of the damaged site is identified as obstructive to repair via the base excision-repair (BER) mechanism. The obstruction can be removed via the enzyme apurinic/apyrimidinic endonuclease I (APE1), thereby enabling repair of hydrolytically damaged DNA via Bst polymerase and Taq ligase. Simulations of damage and repair reveal the benefit of the enzymatic repair step for DNA data storage, especially when data is stored in DNA at high storage densities (=low physical redundancy) and for long time durations. Nature Publishing Group UK 2022-10-20 /pmc/articles/PMC9584896/ /pubmed/36266439 http://dx.doi.org/10.1038/s42003-022-04062-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Meiser, Linda C. Gimpel, Andreas L. Deshpande, Tejas Libort, Gabriela Chen, Weida D. Heckel, Reinhard Nguyen, Bichlien H. Strauss, Karin Stark, Wendelin J. Grass, Robert N. Information decay and enzymatic information recovery for DNA data storage |
title | Information decay and enzymatic information recovery for DNA data storage |
title_full | Information decay and enzymatic information recovery for DNA data storage |
title_fullStr | Information decay and enzymatic information recovery for DNA data storage |
title_full_unstemmed | Information decay and enzymatic information recovery for DNA data storage |
title_short | Information decay and enzymatic information recovery for DNA data storage |
title_sort | information decay and enzymatic information recovery for dna data storage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584896/ https://www.ncbi.nlm.nih.gov/pubmed/36266439 http://dx.doi.org/10.1038/s42003-022-04062-9 |
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