Targeting putative components of the mitochondrial permeability transition pore for novel therapeutics.
Biochem Pharmacol
; 177: 113995, 2020 07.
Article
en En
| MEDLINE
| ID: mdl-32339494
ABSTRACT
Few discoveries have influenced drug discovery programs more than the finding that mitochondrial membranes undergo swings in permeability in response to cellular perturbations. The conductor of these permeability changes is the aptly named mitochondrial permeability transition pore which, although not yet precisely defined, is comprised of several integral proteins that differentially act to regulate the flux of ions, proteins and metabolic byproducts during the course of cellular physiological functions but also pathophysiological insults. Pursuit of the pore's exact identity remains a topic of keen interest, but decades of research have unearthed provocative functions for the integral proteins leading to their evaluation to develop novel therapeutics for a wide range of clinical indications. Chief amongst these targeted, integral proteins have been the Voltage Dependent Anion Channel (VDAC) and the F1FO ATP synthase. Research associated with the roles and ligands of VDAC has been extensive and we will expand upon 3 examples of ligandVDAC interactions for consideration of drug discovery projects TubulinVDAC1, Hexokinase I/IIVDAC1 and olesoximeVDAC1. The discoveries that cyclosporine blocks mitochondrial permeability transition via binding to cyclophilin D, and that cyclophilin D is an important component of F1FO ATP synthase, has heightened interest in the F1FO ATP synthase as a focal point for drug discovery, and we will discuss 2 plausible campaigns associated with disease indications. To date no drug has emerged from prospective targeting these integral proteins; however, continued exploration such as the approaches suggested in this Commentary will increase the likelihood of providing important therapeutics for severely unmet medical needs.
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Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Colestenonas
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Ciclosporina
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Proteínas de Transporte de Membrana Mitocondrial
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Canal Aniónico 1 Dependiente del Voltaje
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Esclerosis Amiotrófica Lateral
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Mitocondrias
Idioma:
En
Revista:
Biochem Pharmacol
Año:
2020
Tipo del documento:
Article