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Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme

[Image: see text] Lipid membranes, enveloping all living systems, are of crucial importance, and control over their structure and composition is a highly desirable functionality of artificial structures. However, the rational design of protein-inspired systems is still challenging. Here we have deve...

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Autores principales: Sobota, Diana, Joshi, Himanshu, Ohmann, Alexander, Aksimentiev, Aleksei, Keyser, Ulrich F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291347/
https://www.ncbi.nlm.nih.gov/pubmed/32374167
http://dx.doi.org/10.1021/acs.nanolett.0c00990
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author Sobota, Diana
Joshi, Himanshu
Ohmann, Alexander
Aksimentiev, Aleksei
Keyser, Ulrich F.
author_facet Sobota, Diana
Joshi, Himanshu
Ohmann, Alexander
Aksimentiev, Aleksei
Keyser, Ulrich F.
author_sort Sobota, Diana
collection PubMed
description [Image: see text] Lipid membranes, enveloping all living systems, are of crucial importance, and control over their structure and composition is a highly desirable functionality of artificial structures. However, the rational design of protein-inspired systems is still challenging. Here we have developed a highly functional nucleic acid construct that self-assembles and inserts into membranes, enabling lipid transfer between inner and outer leaflets. By designing the structure to account for interactions between the DNA, its hydrophobic modifications, and the lipids, we successfully exerted control over the rate of interleaflet lipid transfer induced by our DNA-based enzyme. Furthermore, we can regulate the level of lipid transfer by altering the concentration of divalent ions, similar to stimuli-responsive lipid-flipping proteins.
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spelling pubmed-72913472020-06-15 Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme Sobota, Diana Joshi, Himanshu Ohmann, Alexander Aksimentiev, Aleksei Keyser, Ulrich F. Nano Lett [Image: see text] Lipid membranes, enveloping all living systems, are of crucial importance, and control over their structure and composition is a highly desirable functionality of artificial structures. However, the rational design of protein-inspired systems is still challenging. Here we have developed a highly functional nucleic acid construct that self-assembles and inserts into membranes, enabling lipid transfer between inner and outer leaflets. By designing the structure to account for interactions between the DNA, its hydrophobic modifications, and the lipids, we successfully exerted control over the rate of interleaflet lipid transfer induced by our DNA-based enzyme. Furthermore, we can regulate the level of lipid transfer by altering the concentration of divalent ions, similar to stimuli-responsive lipid-flipping proteins. American Chemical Society 2020-05-06 2020-06-10 /pmc/articles/PMC7291347/ /pubmed/32374167 http://dx.doi.org/10.1021/acs.nanolett.0c00990 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://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 Sobota, Diana
Joshi, Himanshu
Ohmann, Alexander
Aksimentiev, Aleksei
Keyser, Ulrich F.
Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title_full Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title_fullStr Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title_full_unstemmed Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title_short Tailoring Interleaflet Lipid Transfer with a DNA-based Synthetic Enzyme
title_sort tailoring interleaflet lipid transfer with a dna-based synthetic enzyme
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291347/
https://www.ncbi.nlm.nih.gov/pubmed/32374167
http://dx.doi.org/10.1021/acs.nanolett.0c00990
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