Abstract
The 3D structure of the 18-kDa transmembrane (TM) protein TSPO (translocator protein)/PBR (peripheral benzodiazepine receptor), which contains a binding site for benzodiazepines, is important to better understand its function and regulation by endogenous and synthetic ligands. We have recently determined the structure of mammalian TSPO/PBR in complex with the diagnostic ligand PK11195 [1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide; Jaremko et al. (2014) Science 343, 1363-1366], providing for the first time atomic-level insight into the conformation of this protein, which is up-regulated in various pathological conditions including Alzheimer's disease and Parkinson's disease. Here, we review the studies which have probed the structural properties of mammalian TSPO/PBR as well as the homologues bacterial tryptophan-rich sensory proteins (TspOs) over the years and provide detailed insight into the 3D structure of mouse TSPO (mTSPO)/PBR in complex with PK11195.
Original language | English (US) |
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Pages (from-to) | 566-571 |
Number of pages | 6 |
Journal | Biochemical Society Transactions |
Volume | 43 |
DOIs | |
State | Published - Aug 1 2015 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:©2015 Authors; published by Portland Press Limited.
Keywords
- 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide (PK11195)
- Dynamics
- Nuclear magnetic resonance (NMR)
- Peripheral benzodiazepine receptor
- Structure
- TSPO
ASJC Scopus subject areas
- Biochemistry