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Activating ligands of Uncoupling protein 1 identified by rapid membrane protein thermostability shift analysis

Cavalieri, Riccardo (författare)
Klein Hazebroek, Marlou (författare)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Cotrim, Camila A. (författare)
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Lee, Yang (författare)
Kunji, Edmund R. S. (författare)
Jastroch, Martin (författare)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Keipert, Susanne (författare)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Crichton, Paul G. (författare)
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 (creator_code:org_t)
Elsevier BV, 2022
2022
Engelska.
Ingår i: Molecular Metabolism. - : Elsevier BV. - 2212-8778. ; 62
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objective: Uncoupling protein 1 (UCP1) catalyses mitochondrial proton leak in brown adipose tissue to facilitate nutrient oxidation for heat production, and may combat metabolic disease if activated in humans. During the adrenergic stimulation of brown adipocytes, free fatty acids generated from lipolysis activate UCP1 via an unclear interaction. Here, we set out to characterise activator binding to purified UCP1 to clarify the activation process, discern novel activators and the potential to target UCP1.Methods: We assessed ligand binding to purified UCP1 by protein thermostability shift analysis, which unlike many conventional approaches can inform on the binding of hydrophobic ligands to membrane proteins. A detailed activator interaction analysis and screening approach was carried out, supported by investigations of UCP1 activity in liposomes, isolated brown fat mitochondria and UCP1 expression-controlled cell lines.Results: We reveal that fatty acids and other activators influence UCP1 through a specific destabilising interaction, behaving as transport substrates that shift the protein to a less stable conformation of a transport cycle. Through the detection of specific stability shifts in screens, we identify novel activators, including the over-the-counter drug ibuprofen, where ligand analysis indicates that UCP1 has a relatively wide structural specificity for interacting molecules. Ibuprofen successfully induced UCP1 activity in liposomes, isolated brown fat mitochondria and UCP1-expressing HEK293 cells but not in cultured brown adipocytes, suggesting drug delivery differs in each cell type.Conclusions: These findings clarify the nature of the activator-UCP1 interaction and demonstrate that the targeting of UCP1 in cells by approved drugs is in principle achievable as a therapeutic avenue, but requires variants with more effective delivery in brown adipocytes.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

Ligand binding
Thermal stability assay
Differential scanning fluorimetry
Brown adipose tissue
Proton transport
Energy expenditure
Mitochondrial carrier

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