Correction of both NBD1 energetics and domain interface is required to restore Δf508 CFTR folding and function

Wael Rabeh, Florian Bossard, Haijin Xu, Tsukasa Okiyoneda, Miklos Bagdany, Cory M. Mulvihill, Kai Du, Salvatore Di Bernardo, Yuhong Liu, Lars Konermann, Ariel Roldan, Gergely L. Lukacs

Research output: Contribution to journalArticle

Abstract

The folding and misfolding mechanism of multidomain proteins remains poorly understood. Although thermodynamic instability of the first nucleotide-binding domain (NBD1) of ΔF508 CFTR (cystic fibrosis transmembrane conductance regulator) partly accounts for the mutant channel degradation in the endoplasmic reticulum and is considered as a drug target in cystic fibrosis, the link between NBD1 and CFTR misfolding remains unclear. Here, we show that ΔF508 destabilizes NBD1 both thermodynamically and kinetically, but correction of either defect alone is insufficient to restore ΔF508 CFTR biogenesis. Instead, both ΔF508-NBD1 energetic and the NBD1-MSD2 (membrane-spanning domain 2) interface stabilization are required for wild-type-like folding, processing, and transport function, suggesting a synergistic role of NBD1 energetics and topology in CFTR-coupled domain assembly. Identification of distinct structural deficiencies may explain the limited success of ΔF508 CFTR corrector molecules and suggests structure-based combination corrector therapies. These results may serve as a framework for understanding the mechanism of interface mutation in multidomain membrane proteins.

Original languageEnglish (US)
Pages (from-to)150-163
Number of pages14
JournalCell
Volume148
Issue number1-2
DOIs
StatePublished - Jan 20 2012

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Cystic Fibrosis Transmembrane Conductance Regulator
Thermodynamics
Cystic Fibrosis
Endoplasmic Reticulum
Membrane Proteins
Nucleotides
Stabilization
Topology
Membranes
Degradation
Defects
Mutation
Molecules
Processing
Pharmaceutical Preparations
Proteins

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Rabeh, W., Bossard, F., Xu, H., Okiyoneda, T., Bagdany, M., Mulvihill, C. M., ... Lukacs, G. L. (2012). Correction of both NBD1 energetics and domain interface is required to restore Δf508 CFTR folding and function. Cell, 148(1-2), 150-163. https://doi.org/10.1016/j.cell.2011.11.024

Correction of both NBD1 energetics and domain interface is required to restore Δf508 CFTR folding and function. / Rabeh, Wael; Bossard, Florian; Xu, Haijin; Okiyoneda, Tsukasa; Bagdany, Miklos; Mulvihill, Cory M.; Du, Kai; Di Bernardo, Salvatore; Liu, Yuhong; Konermann, Lars; Roldan, Ariel; Lukacs, Gergely L.

In: Cell, Vol. 148, No. 1-2, 20.01.2012, p. 150-163.

Research output: Contribution to journalArticle

Rabeh, W, Bossard, F, Xu, H, Okiyoneda, T, Bagdany, M, Mulvihill, CM, Du, K, Di Bernardo, S, Liu, Y, Konermann, L, Roldan, A & Lukacs, GL 2012, 'Correction of both NBD1 energetics and domain interface is required to restore Δf508 CFTR folding and function', Cell, vol. 148, no. 1-2, pp. 150-163. https://doi.org/10.1016/j.cell.2011.11.024
Rabeh, Wael ; Bossard, Florian ; Xu, Haijin ; Okiyoneda, Tsukasa ; Bagdany, Miklos ; Mulvihill, Cory M. ; Du, Kai ; Di Bernardo, Salvatore ; Liu, Yuhong ; Konermann, Lars ; Roldan, Ariel ; Lukacs, Gergely L. / Correction of both NBD1 energetics and domain interface is required to restore Δf508 CFTR folding and function. In: Cell. 2012 ; Vol. 148, No. 1-2. pp. 150-163.
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