Journal
CHEMISTRY & BIOLOGY
Volume 20, Issue 7, Pages 943-955Publisher
CELL PRESS
DOI: 10.1016/j.chembiol.2013.06.004
Keywords
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Categories
Funding
- FCT, Portugal [PTDC/BIA-BCM/112635/2009]
- European Union [TargetScreen2 EU-LSH-2005-1.2.5-3-037365]
- CFF-Cystic Fibrosis Foundation [7207534]
- FCT [SFRH/BD/35936/2007, SFRH/BPD/74475/2010]
- [PTDC/SAU-GMG/122299/2010]
- [PEst-OE/BIA/UI4046/2011]
- [BioFIG]
- [PEst-OE/EQB/LA0004/2011]
- [ITQB]
- Fundação para a Ciência e a Tecnologia [SFRH/BD/35936/2007, PTDC/BIA-BCM/112635/2009] Funding Source: FCT
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Cystic fibrosis is mostly caused by the F508del mutation, which impairs CFTR protein from exiting the endoplasmic reticulum due to misfolding. VX-809 is a small molecule that rescues F508del-CFTR localization, which recently went into clinical trial but with unknown mechanism of action (MoA). Herein, we assessed if VX-809 is additive or synergistic with genetic revertants of F508del-CFTR, other correctors, and low temperature to determine its MoA. We explored and integrated those various agents in combined treatments, showing how they add to each other to identify their complementary MoA upon correction of F508del-CFTR. Our experimental and modeling data, while compatible with putative binding of VX-809 to NBD1:ICL4 interface, also indicate scope for further synergistic F508del-CFTR correction by other compounds at distinct conformational sites/cellular checkpoints, thus suggesting requirement of combined therapies to fully rescue F508del-CFTR.
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