Login / Signup

A uniquely efficacious type of CFTR corrector with complementary mode of action.

Valentina MarchesinLucile MonnierPeter BlattmannFlorent ChevillardChristine KuntzCamille FornyJudith KamperRolf StuderAlexandre BossuEric A ErtelOliver NaylerChristine BrotschiJodi T WilliamsJohn Gatfield
Published in: Science advances (2024)
Three distinct pharmacological corrector types (I, II, III) with different binding sites and additive behavior only partially rescue the F508del-cystic fibrosis transmembrane conductance regulator (CFTR) folding and trafficking defect observed in cystic fibrosis. We describe uniquely effective, macrocyclic CFTR correctors that were additive to the known corrector types, exerting a complementary "type IV" corrector mechanism. Macrocycles achieved wild-type-like folding efficiency of F508del-CFTR at the endoplasmic reticulum and normalized CFTR currents in reconstituted patient-derived bronchial epithelium. Using photo-activatable macrocycles, docking studies and site-directed mutagenesis a highly probable binding site and pose for type IV correctors was identified in a cavity between lasso helix-1 (Lh1) and transmembrane helix-1 of membrane spanning domain (MSD)-1, distinct from the known corrector binding sites. Since only F508del-CFTR fragments spanning from Lh1 until MSD2 responded to type IV correctors, these likely promote cotranslational assembly of Lh1, MSD1, and MSD2. Previously corrector-resistant CFTR folding mutants were also robustly rescued, suggesting substantial therapeutic potential for type IV correctors.
Keyphrases
  • cystic fibrosis
  • pseudomonas aeruginosa
  • lung function
  • wild type
  • endoplasmic reticulum
  • single molecule
  • crispr cas
  • chronic obstructive pulmonary disease
  • molecular dynamics
  • soft tissue
  • case control