Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A

T. Hegedűs, Andrei Aleksandrov, April Mengos, Liying Cui, Timothy J. Jensen, John R. Riordan

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

The cystic fibrosis transmembrane conductance regulator (CFTR) plays a critical role in transcellular ion transport and when defective, results in the genetic disease cystic fibrosis. CFTR is novel in the ATP-binding cassette superfamily as an ion channel that is enabled by a unique unstructured regulatory domain. This R domain contains multiple protein kinase A sites, which when phosphorylated allow channel gating. Most of the sites have been indicated to stimulate channel activity, while two of them have been suggested to be inhibitory. It is unknown whether individual sites act coordinately or distinctly. To address this issue, we raised monoclonal antibodies recognizing the unphosphorylated, but not the phosphorylated states of four functionally relevant sites (700, 737, 768, and 813). This enabled simultaneous monitoring of their phosphorylation and dephosphorylation and revealed that both processes occurred rapidly at the first three sites, but more slowly at the fourth. The parallel phosphorylation rates of the stimulatory 700 and the putative inhibitory 737 and 768 sites prompted us to reexamine the role of the latter two. With serines 737 and 768 reintroduced individually into a PKA insensitive variant, in which serines at 15 sites had been replaced by alanines, a level of channel activation by PKA was restored, showing that these sites can mediate stimulation. Thus, we have provided new tools to study the CFTR regulation by phosphorylation and found that sites proposed to inhibit channel activity can also participate in stimulation.

Original languageEnglish
Pages (from-to)1341-1349
Number of pages9
JournalBBA - Biomembranes
Volume1788
Issue number6
DOIs
Publication statusPublished - Jun 2009

Fingerprint

Cystic Fibrosis Transmembrane Conductance Regulator
Phosphorylation
Cyclic AMP-Dependent Protein Kinases
Serine
Transcytosis
Inborn Genetic Diseases
Ion Transport
Ion Channels
Cystic Fibrosis
Alanine
Adenosine Triphosphate
Chemical activation
Monoclonal Antibodies
Ions
Monitoring

Keywords

  • ABC protein
  • CFTR
  • Individual phosphorylation site
  • Phosphorylation-sensitive antibody
  • PKA
  • R domain

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Biophysics

Cite this

Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A. / Hegedűs, T.; Aleksandrov, Andrei; Mengos, April; Cui, Liying; Jensen, Timothy J.; Riordan, John R.

In: BBA - Biomembranes, Vol. 1788, No. 6, 06.2009, p. 1341-1349.

Research output: Contribution to journalArticle

Hegedűs, T. ; Aleksandrov, Andrei ; Mengos, April ; Cui, Liying ; Jensen, Timothy J. ; Riordan, John R. / Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A. In: BBA - Biomembranes. 2009 ; Vol. 1788, No. 6. pp. 1341-1349.
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