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Solid-Phase Synthesis of Sequence-Defined Informational Oligomers

[Image: see text] Genetic biopolymers utilize defined sequences and monomer-specific molecular recognition to store and transfer information. Synthetic polymers that mimic these attributes using reversible covalent chemistry for base-pairing pose unique synthetic challenges. Here, we describe a soli...

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Autores principales: Strom, Kyle R., Szostak, Jack W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594334/
https://www.ncbi.nlm.nih.gov/pubmed/33064001
http://dx.doi.org/10.1021/acs.joc.0c01977
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author Strom, Kyle R.
Szostak, Jack W.
author_facet Strom, Kyle R.
Szostak, Jack W.
author_sort Strom, Kyle R.
collection PubMed
description [Image: see text] Genetic biopolymers utilize defined sequences and monomer-specific molecular recognition to store and transfer information. Synthetic polymers that mimic these attributes using reversible covalent chemistry for base-pairing pose unique synthetic challenges. Here, we describe a solid-phase synthesis methodology for the efficient construction of ethynyl benzene oligomers with specific sequences of aniline and benzaldehyde subunits. Handling these oligomers is complicated by the fact that they often exhibit multiple conformations because of intra- or intermolecular pairing. We describe conditions that allow the dynamic behavior of these oligomers to be controlled so that they may be manipulated and characterized without needing to mask the recognition units with protecting groups.
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spelling pubmed-95943342022-10-26 Solid-Phase Synthesis of Sequence-Defined Informational Oligomers Strom, Kyle R. Szostak, Jack W. J Org Chem [Image: see text] Genetic biopolymers utilize defined sequences and monomer-specific molecular recognition to store and transfer information. Synthetic polymers that mimic these attributes using reversible covalent chemistry for base-pairing pose unique synthetic challenges. Here, we describe a solid-phase synthesis methodology for the efficient construction of ethynyl benzene oligomers with specific sequences of aniline and benzaldehyde subunits. Handling these oligomers is complicated by the fact that they often exhibit multiple conformations because of intra- or intermolecular pairing. We describe conditions that allow the dynamic behavior of these oligomers to be controlled so that they may be manipulated and characterized without needing to mask the recognition units with protecting groups. American Chemical Society 2020-10-16 2020-11-06 /pmc/articles/PMC9594334/ /pubmed/33064001 http://dx.doi.org/10.1021/acs.joc.0c01977 Text en © 2020 American Chemical Society https://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.htmlThis is an open access article published under a Creative Commons Attribution (CC-BY) License (https://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Strom, Kyle R.
Szostak, Jack W.
Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title_full Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title_fullStr Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title_full_unstemmed Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title_short Solid-Phase Synthesis of Sequence-Defined Informational Oligomers
title_sort solid-phase synthesis of sequence-defined informational oligomers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594334/
https://www.ncbi.nlm.nih.gov/pubmed/33064001
http://dx.doi.org/10.1021/acs.joc.0c01977
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