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Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose
A fluorescent derivative of trehalose with two dansyl groups (DAT) has been synthesized. It is characterised by a large Stokes shift, good permeability in human living cells and a well detectable fluorescent signal within the cells. Notably, in intestinal cells DAT is sequestered in vesicles induced...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064201/ https://www.ncbi.nlm.nih.gov/pubmed/35514834 http://dx.doi.org/10.1039/c9ra01800j |
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author | Locatelli, Alessandra Iommarini, Luisa Graziadio, Alessandra Leoni, Alberto Porcelli, Anna Maria Iotti, Stefano Malucelli, Emil Francia, Francesco Venturoli, Giovanni Farruggia, Giovanna |
author_facet | Locatelli, Alessandra Iommarini, Luisa Graziadio, Alessandra Leoni, Alberto Porcelli, Anna Maria Iotti, Stefano Malucelli, Emil Francia, Francesco Venturoli, Giovanni Farruggia, Giovanna |
author_sort | Locatelli, Alessandra |
collection | PubMed |
description | A fluorescent derivative of trehalose with two dansyl groups (DAT) has been synthesized. It is characterised by a large Stokes shift, good permeability in human living cells and a well detectable fluorescent signal within the cells. Notably, in intestinal cells DAT is sequestered in vesicles induced by trehalose pre-treatment and colocalizes with lipid droplets. |
format | Online Article Text |
id | pubmed-9064201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90642012022-05-04 Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose Locatelli, Alessandra Iommarini, Luisa Graziadio, Alessandra Leoni, Alberto Porcelli, Anna Maria Iotti, Stefano Malucelli, Emil Francia, Francesco Venturoli, Giovanni Farruggia, Giovanna RSC Adv Chemistry A fluorescent derivative of trehalose with two dansyl groups (DAT) has been synthesized. It is characterised by a large Stokes shift, good permeability in human living cells and a well detectable fluorescent signal within the cells. Notably, in intestinal cells DAT is sequestered in vesicles induced by trehalose pre-treatment and colocalizes with lipid droplets. The Royal Society of Chemistry 2019-05-16 /pmc/articles/PMC9064201/ /pubmed/35514834 http://dx.doi.org/10.1039/c9ra01800j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Locatelli, Alessandra Iommarini, Luisa Graziadio, Alessandra Leoni, Alberto Porcelli, Anna Maria Iotti, Stefano Malucelli, Emil Francia, Francesco Venturoli, Giovanni Farruggia, Giovanna Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title_full | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title_fullStr | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title_full_unstemmed | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title_short | Dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
title_sort | dansyl acetyl trehalose: a novel tool to investigate the cellular fate of trehalose |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064201/ https://www.ncbi.nlm.nih.gov/pubmed/35514834 http://dx.doi.org/10.1039/c9ra01800j |
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