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The still uncertain identity of the channel-forming unit(s) of the mitochondrial permeability transition pore
Affiliation:1. Department of Herbology, School of Oriental Medicine, Wonkwang University, Iksan, Jeonbuk 54538, South Korea;2. Hanbang Cardio-Renal Syndrome Research Center, Wonkwang University, Iksan, Jeonbuk 54538, South Korea;3. Division of Beauty Sciences, School of Natural Sciences, Wonkwang University, Iksan, Jeonbuk 54538, South Korea;4. School of Korean Medicine, Pusan National University, Yangsan 50621, South Korea
Abstract:Mitochondria from different organisms can undergo a sudden process of inner membrane unselective leakiness to molecules known as the mitochondrial permeability transition (MPT). This process has been studied for nearly four decades and several proteins have been claimed to constitute, or at least regulate the usually inactive pore responsible for this transition. However, no protein candidate proposed as the actual pore-forming unit has passed rigorous gain- or loss-of-function genetic tests. Here we review evidence for -and against- putative channel-forming components of the MPT pore. We conclude that the structure of the MPT pore still remains largely undefined and suggest that future studies should follow established technical considerations to unambiguously consolidate the channel forming constituent(s) of the MPT pore.
Keywords:Mitochondrial permeability transition pore  Phosphate carrier  ATP synthase  Adenine nucleotide translocase  Cyclophilin D  Bioenergetics  Cell death  Cyclosporin A
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