In this issue of the Biochemical Journal, Zhang et al. reveal a new strategy for modifying the regulated function of CFTR (cystic fibrosis transmembrane conductance regulator) on the apical surface of epithelial cells. Simply stated, these authors tested the idea that the cAMP-dependent channel activity of CFTR could be effectively enhanced by disruption of a protein–protein interaction which is normally inhibitory for the production of cAMP. This particular protein–protein interaction [between the PDZ motif of LPA2 (type 2 lysophosphatidic acid receptor) and the scaffold protein Nherf2 (Na+/H+ exchanger regulatory factor 2)] is localized in the CFTR interactome on the apical membrane of epithelial cells. Hence disruption of the LPA2–Nherf2 interaction should lead to a localized elevation in cAMP and, consequently, increased cAMP-dependent CFTR activity on the surface of epithelial cells. Zhang et al. confirmed these expectations for a small-molecule compound targeting the LPA2–Nherf2 interaction using relevant cultures and tissues thought to model the human respiratory epithelium. The success of this strategy depended on previous knowledge regarding the role for multiple PDZ-motif-mediated interactions in signalling (directly or indirectly) to CFTR. Given the number and diversity of such PDZ-mediated interactions, future structural and computational studies will be essential for guiding the design of specific pharmacological interventions.
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March 29 2011
Targeting the regulation of CFTR channels
Paul D.W. Eckford;
Paul D.W. Eckford
1Programme in Molecular Structure and Function in the Research Institute, The Hospital for Sick Children and the Departments of Biochemistry and Physiology, The University of Toronto, 555 University Avenue, Toronto, Ontario, Canada, MG5 1X8
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Christine E. Bear
Christine E. Bear
1
1Programme in Molecular Structure and Function in the Research Institute, The Hospital for Sick Children and the Departments of Biochemistry and Physiology, The University of Toronto, 555 University Avenue, Toronto, Ontario, Canada, MG5 1X8
1To whom correspondence should be addressed (email bear@sickkids.ca).
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Publisher: Portland Press Ltd
Received:
March 10 2011
Accepted:
March 11 2011
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© The Authors Journal compilation © 2011 Biochemical Society
2011
Biochem J (2011) 435 (2): e1–e4.
Article history
Received:
March 10 2011
Accepted:
March 11 2011
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Citation
Paul D.W. Eckford, Christine E. Bear; Targeting the regulation of CFTR channels. Biochem J 15 April 2011; 435 (2): e1–e4. doi: https://doi.org/10.1042/BJ20110461
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