New insights into interactions between the nucleotide‐binding domain of CFTR and keratin 8 |
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Authors: | Arkadiusz Bonna Grazyna Faure Tomasz Fraczyk Ariel Roldan Brice Hoffmann Mélanie Faria da Cunha Harald Herrmann Gergely L. Lukacs Aleksander Edelman Michał Dadlez |
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Affiliation: | 1. Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Poland;2. Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom;3. Unité Récepteurs‐Canaux;4. Institut Pasteur, CNRS, URA 2182, Paris, France;5. Department of Physiology, McGill University, Montreal, QC, Canada;6. IMPMC, Sorbonne Universités, UPMC Université Paris 06, UMR CNRS 7590, Museum National d'Histoire Naturelle, IRD UMR 206, IUC, Paris Cedex 05, France;7. INSERM U1151, team Canalopathies épithéliales : la mucoviscidose et autres maladies, Université Paris Descartes, Paris, France;8. Department of Molecular Genetics, German Cancer Research Center, Heidelberg, Germany;9. Institute of Neuropathology, University Hospital Erlangen, Erlangen, Germany |
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Abstract: | The intermediate filament protein keratin 8 (K8) interacts with the nucleotide‐binding domain 1 (NBD1) of the cystic fibrosis (CF) transmembrane regulator (CFTR) with phenylalanine 508 deletion (ΔF508), and this interaction hampers the biogenesis of functional ΔF508‐CFTR and its insertion into the plasma membrane. Interruption of this interaction may constitute a new therapeutic target for CF patients bearing the ΔF508 mutation. Here, we aimed to determine the binding surface between these two proteins, to facilitate the design of the interaction inhibitors. To identify the NBD1 fragments perturbed by the ΔF508 mutation, we used hydrogen–deuterium exchange coupled with mass spectrometry (HDX‐MS) on recombinant wild‐type (wt) NBD1 and ΔF508‐NBD1 of CFTR. We then performed the same analysis in the presence of a peptide from the K8 head domain, and extended this investigation using bioinformatics procedures and surface plasmon resonance, which revealed regions affected by the peptide binding in both wt‐NBD1 and ΔF508‐NBD1. Finally, we performed HDX‐MS analysis of the NBD1 molecules and full‐length K8, revealing hydrogen‐bonding network changes accompanying complex formation. In conclusion, we have localized a region in the head segment of K8 that participates in its binding to NBD1. Our data also confirm the stronger binding of K8 to ΔF508‐NBD1, which is supported by an additional binding site located in the vicinity of the ΔF508 mutation in NBD1. |
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Keywords: | cystic fibrosis CFTR keratin 8 NBD1 hydrogen‐deuterium exchange mass spectrometry protein structure |
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