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Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker

Multistep synthesis in the laboratory typically requires numerous reaction vessels, each containing a different set of reactants. In contrast, cells are capable of performing highly efficient and selective multistep biosynthesis under mild conditions with all reactants simultaneously present in solu...

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Detalles Bibliográficos
Autores principales: He, Yu, Liu, David R.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974042/
https://www.ncbi.nlm.nih.gov/pubmed/20935654
http://dx.doi.org/10.1038/nnano.2010.190
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author He, Yu
Liu, David R.
author_facet He, Yu
Liu, David R.
author_sort He, Yu
collection PubMed
description Multistep synthesis in the laboratory typically requires numerous reaction vessels, each containing a different set of reactants. In contrast, cells are capable of performing highly efficient and selective multistep biosynthesis under mild conditions with all reactants simultaneously present in solution. If the latter approach could be applied in the laboratory, it may improve the ease, speed, and efficiency of multistep reaction sequences. Here we show that a DNA mechanical device— a DNA walker moving along a DNA track— can be used to perform a series of amine acylation reactions in a single solution without any external intervention. The multistep products generated by this primitive ribosome mimetic are programmed by the sequence of the DNA track, are unrelated to the structure of DNA, and are formed with speeds and overall yields significantly greater than those previously achieved by multistep DNA-templated small-molecule synthesis.
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spelling pubmed-29740422011-05-01 Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker He, Yu Liu, David R. Nat Nanotechnol Article Multistep synthesis in the laboratory typically requires numerous reaction vessels, each containing a different set of reactants. In contrast, cells are capable of performing highly efficient and selective multistep biosynthesis under mild conditions with all reactants simultaneously present in solution. If the latter approach could be applied in the laboratory, it may improve the ease, speed, and efficiency of multistep reaction sequences. Here we show that a DNA mechanical device— a DNA walker moving along a DNA track— can be used to perform a series of amine acylation reactions in a single solution without any external intervention. The multistep products generated by this primitive ribosome mimetic are programmed by the sequence of the DNA track, are unrelated to the structure of DNA, and are formed with speeds and overall yields significantly greater than those previously achieved by multistep DNA-templated small-molecule synthesis. 2010-10-10 2010-11 /pmc/articles/PMC2974042/ /pubmed/20935654 http://dx.doi.org/10.1038/nnano.2010.190 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
He, Yu
Liu, David R.
Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title_full Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title_fullStr Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title_full_unstemmed Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title_short Autonomous Multistep Organic Synthesis in a Single Isothermal Solution Mediated by a DNA Walker
title_sort autonomous multistep organic synthesis in a single isothermal solution mediated by a dna walker
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974042/
https://www.ncbi.nlm.nih.gov/pubmed/20935654
http://dx.doi.org/10.1038/nnano.2010.190
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