
doi: 10.1007/bf00769532
pmid: 1380506
Specific, high-affinity receptors for numerous drugs have recently been localized to mitochondrial membrane proteins. This review discusses the association of the mitochondrial receptor for benzodiazepines (mBzR) with the voltage-dependent anion channel (VDAC), indicating a possible auxiliary role for VDAC as a putative drug binding protein. The proposed subunit composition of the purified mBzR complex isolated from rat kidney mitochondria includes VDAC, which functions as a recognition site for benzodiazepines (e.g., flunitrazepam), the adenine nucleotide carrier (ADC), and an 18 kDa outer membrane protein identified by covalent labelling with the mBzR antagonists isoquinoline carboxamides (e.g., PK14105).
Animals, Membrane Proteins, Porins, Voltage-Dependent Anion Channels, Receptors, GABA-A, Ion Channels, Mitochondria
Animals, Membrane Proteins, Porins, Voltage-Dependent Anion Channels, Receptors, GABA-A, Ion Channels, Mitochondria
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