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Multicomponent molecular memory
Multicomponent reactions enable the synthesis of large molecular libraries from relatively few inputs. This scalability has led to the broad adoption of these reactions by the pharmaceutical industry. Here, we employ the four-component Ugi reaction to demonstrate that multicomponent reactions can pr...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000828/ https://www.ncbi.nlm.nih.gov/pubmed/32019933 http://dx.doi.org/10.1038/s41467-020-14455-1 |
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author | Arcadia, Christopher E. Kennedy, Eamonn Geiser, Joseph Dombroski, Amanda Oakley, Kady Chen, Shui-Ling Sprague, Leonard Ozmen, Mustafa Sello, Jason Weber, Peter M. Reda, Sherief Rose, Christopher Kim, Eunsuk Rubenstein, Brenda M. Rosenstein, Jacob K. |
author_facet | Arcadia, Christopher E. Kennedy, Eamonn Geiser, Joseph Dombroski, Amanda Oakley, Kady Chen, Shui-Ling Sprague, Leonard Ozmen, Mustafa Sello, Jason Weber, Peter M. Reda, Sherief Rose, Christopher Kim, Eunsuk Rubenstein, Brenda M. Rosenstein, Jacob K. |
author_sort | Arcadia, Christopher E. |
collection | PubMed |
description | Multicomponent reactions enable the synthesis of large molecular libraries from relatively few inputs. This scalability has led to the broad adoption of these reactions by the pharmaceutical industry. Here, we employ the four-component Ugi reaction to demonstrate that multicomponent reactions can provide a basis for large-scale molecular data storage. Using this combinatorial chemistry we encode more than 1.8 million bits of art historical images, including a Cubist drawing by Picasso. Digital data is written using robotically synthesized libraries of Ugi products, and the files are read back using mass spectrometry. We combine sparse mixture mapping with supervised learning to achieve bit error rates as low as 0.11% for single reads, without library purification. In addition to improved scaling of non-biological molecular data storage, these demonstrations offer an information-centric perspective on the high-throughput synthesis and screening of small-molecule libraries. |
format | Online Article Text |
id | pubmed-7000828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70008282020-02-06 Multicomponent molecular memory Arcadia, Christopher E. Kennedy, Eamonn Geiser, Joseph Dombroski, Amanda Oakley, Kady Chen, Shui-Ling Sprague, Leonard Ozmen, Mustafa Sello, Jason Weber, Peter M. Reda, Sherief Rose, Christopher Kim, Eunsuk Rubenstein, Brenda M. Rosenstein, Jacob K. Nat Commun Article Multicomponent reactions enable the synthesis of large molecular libraries from relatively few inputs. This scalability has led to the broad adoption of these reactions by the pharmaceutical industry. Here, we employ the four-component Ugi reaction to demonstrate that multicomponent reactions can provide a basis for large-scale molecular data storage. Using this combinatorial chemistry we encode more than 1.8 million bits of art historical images, including a Cubist drawing by Picasso. Digital data is written using robotically synthesized libraries of Ugi products, and the files are read back using mass spectrometry. We combine sparse mixture mapping with supervised learning to achieve bit error rates as low as 0.11% for single reads, without library purification. In addition to improved scaling of non-biological molecular data storage, these demonstrations offer an information-centric perspective on the high-throughput synthesis and screening of small-molecule libraries. Nature Publishing Group UK 2020-02-04 /pmc/articles/PMC7000828/ /pubmed/32019933 http://dx.doi.org/10.1038/s41467-020-14455-1 Text en © 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/. |
spellingShingle | Article Arcadia, Christopher E. Kennedy, Eamonn Geiser, Joseph Dombroski, Amanda Oakley, Kady Chen, Shui-Ling Sprague, Leonard Ozmen, Mustafa Sello, Jason Weber, Peter M. Reda, Sherief Rose, Christopher Kim, Eunsuk Rubenstein, Brenda M. Rosenstein, Jacob K. Multicomponent molecular memory |
title | Multicomponent molecular memory |
title_full | Multicomponent molecular memory |
title_fullStr | Multicomponent molecular memory |
title_full_unstemmed | Multicomponent molecular memory |
title_short | Multicomponent molecular memory |
title_sort | multicomponent molecular memory |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000828/ https://www.ncbi.nlm.nih.gov/pubmed/32019933 http://dx.doi.org/10.1038/s41467-020-14455-1 |
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