Preferential phosphorylation of R-domain Serine 768 dampens activation of CFTR channels by PKA

• Published in: The Journal of general physiology 2005-02, Vol.125 (2), p.171-186
• Main Authors: Csanády, László, Seto-Young, Donna, Chan, Kim W, Cenciarelli, Cristina, Angel, Benjamin B, Qin, Jun, McLachlin, Derek T, Krutchinsky, Andrew N, Chait, Brian T, Nairn, Angus C, Gadsby, David C
• Format: Article
• Language: English
• Subjects: ABC transporters; Amino acids; Animals; ATP-Binding Cassette Transporters - physiology; Autoradiography; Biochemistry; Chlorine; Cyclic AMP-Dependent Protein Kinases - pharmacology; Cystic fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator - metabolism; Cystic Fibrosis Transmembrane Conductance Regulator - physiology; Female; Humans; Ion Channel Gating - physiology; Ions; Kinetics; Mass Spectrometry; Oocytes; Phosphorylation; Proteins; Serine - metabolism; Xenopus
• ISSN: 0022-1295; 1540-7748
• DOI: 10.1085/jgp.200409076

CFTR (cystic fibrosis transmembrane conductance regulator), the protein whose dysfunction causes cystic fibrosis, is a chloride ion channel whose gating is controlled by interactions of MgATP with CFTR's two cytoplasmic nucleotide binding domains, but only after several serines in CFTR's regulatory (R) domain have been phosphorylated by cAMP-dependent protein kinase (PKA). Whereas eight R-domain serines have previously been shown to be phosphorylated in purified CFTR, it is not known how individual phosphoserines regulate channel gating, although two of them, at positions 737 and 768, have been suggested to be inhibitory. Here we show, using mass spectrometric analysis, that Ser 768 is the first site phosphorylated in purified R-domain protein, and that it and five other R-domain sites are already phosphorylated in resting Xenopus oocytes expressing wild-type (WT) human epithelial CFTR. The WT channels have lower activity than S768A channels (with Ser 768 mutated to Ala) in resting oocytes, confirming the inhibitory influence of phosphoserine 768. In excised patches exposed to a range of PKA concentrations, the open probability (P(o)) of mutant S768A channels exceeded that of WT CFTR channels at all [PKA], and the half-maximally activating [PKA] for WT channels was twice that for S768A channels. As the open burst duration of S768A CFTR channels was almost double that of WT channels, at both low (55 nM) and high (550 nM) [PKA], we conclude that the principal mechanism by which phosphoserine 768 inhibits WT CFTR is by hastening the termination of open channel bursts. The right-shifted P(o)-[PKA] curve of WT channels might explain their slower activation, compared with S768A channels, at low [PKA]. The finding that phosphorylation kinetics of WT or S768A R-domain peptides were similar provides no support for an alternative explanation, that early phosphorylation of Ser 768 in WT CFTR might also impair subsequent phosphorylation of stimulatory R-domain serines. The observed reduced sensitivity to activation by [PKA] imparted by Ser 768 might serve to ensure activation of WT CFTR by strong stimuli while dampening responses to weak signals.