Monitoring and Modulating Intracellular Cholesterol Trafficking Using ALOD4, a Cholesterol-Binding Protein.
Anthrolysin O
Cholesterol trafficking
Endoplasmic reticulum
Plasma membrane
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
22
2
2019
pubmed:
23
2
2019
medline:
16
7
2019
Statut:
ppublish
Résumé
Mammalian cells carefully control their cholesterol levels by employing multiple feedback mechanisms to regulate synthesis of cholesterol and uptake of cholesterol from circulating lipoproteins. Most of a cell's cholesterol (~80% of total) is in the plasma membrane (PM), but the protein machinery that regulates cellular cholesterol resides in the endoplasmic reticulum (ER) membrane, which contains a very small fraction (~1% of total) of a cell's cholesterol. How does the ER communicate with PM to monitor cholesterol levels in that membrane? Here, we describe a tool, ALOD4, that helps us answer this question. ALOD4 traps cholesterol at the PM, leading to depletion of ER cholesterol without altering total cell cholesterol. The effects of ALOD4 are reversible. This tool has been used to show that the ER is able to continuously sample cholesterol from PM, providing ER with information about levels of PM cholesterol.
Identifiants
pubmed: 30790255
doi: 10.1007/978-1-4939-9136-5_12
pmc: PMC6459602
mid: NIHMS1014654
doi:
Substances chimiques
Carrier Proteins
0
Cholesterol
97C5T2UQ7J
Pancreatic Elastase
EC 3.4.21.36
cholesterol-binding protein
EC 3.4.21.36
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
153-163Subventions
Organisme : NHLBI NIH HHS
ID : P01 HL020948
Pays : United States
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