Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2683
Title: Uncoupling proteins : Martin Klingenberg's contributions for 40 years
Authors: Echtay, Karim 
Bienengraeber, Martin
Mayinger, Peter
Heimpel, Simone
Winkler, Edith
Druhmann, Doerthe
Frischmuth, Karina
Kamp, Frits
Huang, Shu-Gui
Affiliations: Faculty of Medicine 
Keywords: Uncoupling protein
Non-shivering thermogenesis
Brown adipose tissue
Solute transport
Drug discovery
Subjects: Mitochondria
Obesity
Issue Date: 2018
Part of: Journal of archives of biochemistry and biophysics
Volume: 657
Start page: 41
End page: 55
Abstract: 
The uncoupling protein (UCP1) is a proton (H+) transporter in the mitochondrial inner membrane. By dissipating the electrochemical H+ gradient, UCP1 uncouples respiration from ATP synthesis, which drives an increase in substrate oxidation via the TCA cycle flux that generates more heat. The mitochondrial uncoupling-mediated non-shivering thermogenesis in brown adipose tissue is vital primarily to mammals, such as rodents and new-born humans, but more recently additional functions in adult humans have been described. UCP1 is regulated by β-adrenergic receptors through the sympathetic nervous system and at the molecular activity level by nucleotides and fatty acid to meet thermogenesis needs. The discovery of novel UCP homologs has greatly contributed to the understanding of human diseases, such as obesity and diabetes. In this article, we review the progress made towards the molecular mechanism and function of the UCPs, in particular focusing on the influential contributions from Martin Klingenberg's laboratory. Because all members of the UCP family are potentially promising drug targets, we also present and discuss possible approaches and methods for UCP-related drug discovery.
URI: https://scholarhub.balamand.edu.lb/handle/uob/2683
DOI: 10.1016/j.abb.2018.09.006
Ezproxy URL: Link to full text
Type: Journal Article
Appears in Collections:Faculty of Medicine

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