Tadalafil Rescues the p.M325T Mutant of Best1 Chloride Channel.
Kathleen ElversonJim WarwickerSally FreemanForbes MansonPublished in: Molecules (Basel, Switzerland) (2023)
Bestrophin 1 (Best1) is a chloride channel that localises to the plasma membrane of retinal pigment epithelium (RPE) cells. Mutations in the BEST1 gene are associated with a group of untreatable inherited retinal dystrophies (IRDs) called bestrophinopathies, caused by protein instability and loss-of-function of the Best1 protein. 4PBA and 2-NOAA have been shown to rescue the function, expression, and localisation of Best1 mutants; however, it is of interest to find more potent analogues as the concentration of the drugs required is too high (2.5 mM) to be given therapeutically. A virtual docking model of the COPII Sec24a site, where 4PBA has been shown to bind, was generated and a library of 1416 FDA-approved compounds was screened at the site. The top binding compounds were tested in vitro in whole-cell patch-clamp experiments of HEK293T cells expressing mutant Best1. The application of 25 μM tadalafil resulted in full rescue of Cl - conductance, comparable to wild type Best1 levels, for p.M325T mutant Best1 but not for p.R141H or p.L234V mutants.
Keyphrases
- wild type
- protein protein
- binding protein
- induced apoptosis
- poor prognosis
- optical coherence tomography
- single cell
- small molecule
- amino acid
- molecular dynamics
- molecular dynamics simulations
- copy number
- cell cycle arrest
- signaling pathway
- mouse model
- molecular docking
- diabetic retinopathy
- cell therapy
- dna methylation
- mesenchymal stem cells
- drug administration
- anti inflammatory
- dna binding