Identification of the major phosphorylation domain of murine mdr1b P-glycoprotein: Analysis of the protein kinase A and protein kinase C phosphorylation sites

George A. Orr, Edward K.H. Han, Paul C. Browne, Edward Nieves, Brigid M. O'Connort, Chia Ping Huang Yang, Susan Band Horwitz

Research output: Contribution to journalArticlepeer-review

67 Scopus citations


P-glycoprotein is phosphorylated in cells, and it has been suggested that phosphorylation may regulate the drug transport activity of P-glycoprotein. Domain mapping, utilizing a combination of cyanogen bromide digestion and immunoblot analysis, was used to reveal the major phosphorylation sites in murine mdrlb P-glycoprotein. After labeling of J7.V1-1 cells with [32P]Pi, or labeling membranes with [γ-32P]ATP and either protein kinase A or protein kinase C, it was found that the majority of the label was contained within a single cyanogen bromide fragment (amino acid 627-682) that encompassed the majority of the linker region. The in vitro protein kinase C phosphorylation sites within this fragment were analyzed by a combination of fast atom bombardment mass spectrometry (FABMS) and two-dimensional phosphopeptide mapping. FABMS analysis of a protein kinase C-phosphorylated synthetic peptide, corresponding to a segment of the linker region of P-glycoprotein, identified serine 669 as the single site of phosphorylation. Comparison of two-dimensional tryptic phosphopeptide maps prepared from synthetic peptide and P-glycoprotein, both of which were phosphorylated in vitro with protein kinase C, revealed that serine 669 was also the major phosphorylation site in the intact glycoprotein. The in vitro protein kinase A phosphorylation site was identified as serine 681 by site-directed mutagenesis. Inspection of the gene organization and the deduced amino acid sequence of mdr1b P-glycoprotein revealed that the linker region, although shorter than the R domain (55 versus 241 amino acids), fits the operational definition of the R domain of cystic fibrosis conductance regulator. Like the R domain, the linker region is encoded by a single exon, is highly charged with alternating acidic and basic side chains, and contains several protein kinase A/protein kinase C consensus phosphorylation sites. Since the R domain is believed to be involved in the regulation of cystic fibrosis conductance regulator function by phosphorylation, it is possible that the linker region plays a similar regulatory role in P-glycoprotein function.

Original languageEnglish (US)
Pages (from-to)25054-25062
Number of pages9
JournalJournal of Biological Chemistry
Issue number33
StatePublished - Nov 25 1993

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology


Dive into the research topics of 'Identification of the major phosphorylation domain of murine mdr1b P-glycoprotein: Analysis of the protein kinase A and protein kinase C phosphorylation sites'. Together they form a unique fingerprint.

Cite this