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DNA-Programmed Lipid Nanoreactors for Synthesis of Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments
[Image: see text] Lipid nanoreactors are biomimetic reaction vessels (nanoreactors) that can host aqueous or membrane-associated chemical and enzymatic reactions. Nanoreactors provide ultra-miniaturization from atto- to zeptoliter volumes per reaction vessel with the major challenge of encoding and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510321/ https://www.ncbi.nlm.nih.gov/pubmed/37619973 http://dx.doi.org/10.1021/jacs.3c04093 |
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author | Tian, Xinwei Risgaard, Nikolaj Alexander Löffler, Philipp M. G. Vogel, Stefan |
author_facet | Tian, Xinwei Risgaard, Nikolaj Alexander Löffler, Philipp M. G. Vogel, Stefan |
author_sort | Tian, Xinwei |
collection | PubMed |
description | [Image: see text] Lipid nanoreactors are biomimetic reaction vessels (nanoreactors) that can host aqueous or membrane-associated chemical and enzymatic reactions. Nanoreactors provide ultra-miniaturization from atto- to zeptoliter volumes per reaction vessel with the major challenge of encoding and spatio-temporal control over reactions at the individual nanoreactor or population level, thereby controlling volumes several orders of magnitude below advanced microfluidic devices. We present DNA-programmed lipid nanoreactors (PLNs) functionalized with lipidated oligonucleotides (LiNAs) that allow programming and encoding of nanoreactor interactions by controlled membrane fusion, exemplified for a set of carbohydrate mimetics with mono- to hexasaccharide azide building blocks connected by click-chemistry. Programmed reactions are initiated by fusion of distinct populations of nanoreactors with individually encapsulated building blocks. A focused library of triazole-linked carbohydrate-Cy5 conjugates formed by strain-promoted azide-alkyne cycloadditions demonstrated LiNA-programmed chemistry, including two-step reaction schemes. The PLN method is developed toward a robust platform for synthesis in confined space employing fully programmable nanoreactors, applicable to multistep synthesis for the generation of combinatorial libraries with subsequent analysis of the molecules formed, based on the addressability of the lipid nanoreactors. |
format | Online Article Text |
id | pubmed-10510321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105103212023-09-21 DNA-Programmed Lipid Nanoreactors for Synthesis of Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments Tian, Xinwei Risgaard, Nikolaj Alexander Löffler, Philipp M. G. Vogel, Stefan J Am Chem Soc [Image: see text] Lipid nanoreactors are biomimetic reaction vessels (nanoreactors) that can host aqueous or membrane-associated chemical and enzymatic reactions. Nanoreactors provide ultra-miniaturization from atto- to zeptoliter volumes per reaction vessel with the major challenge of encoding and spatio-temporal control over reactions at the individual nanoreactor or population level, thereby controlling volumes several orders of magnitude below advanced microfluidic devices. We present DNA-programmed lipid nanoreactors (PLNs) functionalized with lipidated oligonucleotides (LiNAs) that allow programming and encoding of nanoreactor interactions by controlled membrane fusion, exemplified for a set of carbohydrate mimetics with mono- to hexasaccharide azide building blocks connected by click-chemistry. Programmed reactions are initiated by fusion of distinct populations of nanoreactors with individually encapsulated building blocks. A focused library of triazole-linked carbohydrate-Cy5 conjugates formed by strain-promoted azide-alkyne cycloadditions demonstrated LiNA-programmed chemistry, including two-step reaction schemes. The PLN method is developed toward a robust platform for synthesis in confined space employing fully programmable nanoreactors, applicable to multistep synthesis for the generation of combinatorial libraries with subsequent analysis of the molecules formed, based on the addressability of the lipid nanoreactors. American Chemical Society 2023-08-24 /pmc/articles/PMC10510321/ /pubmed/37619973 http://dx.doi.org/10.1021/jacs.3c04093 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Tian, Xinwei Risgaard, Nikolaj Alexander Löffler, Philipp M. G. Vogel, Stefan DNA-Programmed Lipid Nanoreactors for Synthesis of Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title | DNA-Programmed Lipid
Nanoreactors for Synthesis of
Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title_full | DNA-Programmed Lipid
Nanoreactors for Synthesis of
Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title_fullStr | DNA-Programmed Lipid
Nanoreactors for Synthesis of
Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title_full_unstemmed | DNA-Programmed Lipid
Nanoreactors for Synthesis of
Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title_short | DNA-Programmed Lipid
Nanoreactors for Synthesis of
Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments |
title_sort | dna-programmed lipid
nanoreactors for synthesis of
carbohydrate mimetics by fusion of aqueous sub-attoliter compartments |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510321/ https://www.ncbi.nlm.nih.gov/pubmed/37619973 http://dx.doi.org/10.1021/jacs.3c04093 |
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