Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation.

Journal Article (Journal Article)

We have designed and synthesized benzo[c]quinolizinium derivatives and evaluated their effects on the activity of G551D cystic fibrosis transmembrane conductance regulator (CFTR) expressed in Chinese hamster ovary and Fisher rat thyroid cells. We demonstrated, using iodide efflux, whole cell patch clamp, and short-circuit recordings, that 5-butyl-6-hydroxy-10-chlorobenzo[c]quinolizinium chloride (MPB-91) restored the activity of G551D CFTR (EC(50) = 85 microM) and activated CFTR in Calu-3 cells (EC(50) = 47 microM). MPB-91 has no effect on the ATPase activity of wild-type and G551D NBD1/R/GST fusion proteins or on the ATPase, GTPase, and adenylate kinase activities of purified NBD2. The activation of CFTR by MPB-91 is independent of phosphorylation because 1) kinase inhibitors have no effect and 2) the compound still activated CFTR having 10 mutated protein kinase A sites (10SA-CFTR). The new pharmacological agent MPB-91 may be an important candidate drug to ameliorate the ion transport defect associated with CF and to point out a new pathway to modulate CFTR activity.

Full Text

Duke Authors

Cited Authors

  • Dérand, R; Bulteau-Pignoux, L; Mettey, Y; Zegarra-Moran, O; Howell, LD; Randak, C; Galietta, LJ; Cohn, JA; Norez, C; Romio, L; Vierfond, JM; Joffre, M; Becq, F

Published Date

  • November 2001

Published In

Volume / Issue

  • 281 / 5

Start / End Page

  • C1657 - C1666

PubMed ID

  • 11600430

International Standard Serial Number (ISSN)

  • 0363-6143

Digital Object Identifier (DOI)

  • 10.1152/ajpcell.2001.281.5.C1657


  • eng

Conference Location

  • United States