Synthesis and biological evaluation of cationic TopFluor cholesterol analogues
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
34700109
DOI
10.1016/j.bioorg.2021.105410
PII: S0045-2068(21)00787-2
Knihovny.cz E-resources
- Keywords
- Cholesterol transport, Fluorescence imaging, Sterol, TopFluor cholesterol analogues, Trafficking disorders,
- MeSH
- Biological Transport MeSH
- Cell Line MeSH
- Cholesterol analogs & derivatives analysis chemical synthesis metabolism MeSH
- Humans MeSH
- Optical Imaging MeSH
- Boron Compounds analysis chemical synthesis chemistry metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene MeSH Browser
- Cholesterol MeSH
- Boron Compounds MeSH
Cholesterol is not only a major component of the cell membrane, but also plays an important role in a wide range of biological processes and pathologies. It is therefore crucial to develop appropriate tools for visualizing intracellular cholesterol transport. Here, we describe new cationic analogues of BODIPY-Cholesterol (TopFluor-Cholesterol, TF-Chol), which combine a positive charge on the sterol side chain and a BODIPY group connected via a C-4 linker. In contrast to TF-Chol, the new analogues TF-1 and TF-3 possessing acetyl groups on the A ring (C-3 position on steroid) internalized much faster and displayed slightly different levels of intracellular localization. Their applicability for cholesterol monitoring was indicated by the fact that they strongly label compartments with accumulated cholesterol in cells carrying a mutation of the Niemann-Pick disease-associated cholesterol transporter, NPC1.
Czech University of Life Sciences Prague Kamýcká 129 165 00 Prague 6 Czech Republic
University of Chemistry and Technology Technická 5 166 28 Prague 6 Czech Republic
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