Winstel R, Freund S, Krasel C, Hoppe E, Lohse M J
Laboratory of Molecular Biology, University of Munich, Germany.
Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2105-9. doi: 10.1073/pnas.93.5.2105.
The beta-adrenergic receptor kinase (betaARK) is the prototypical member of the family of cytosolic kinases that phosphorylate guanine nucleotide binding-protein-coupled receptors and thereby trigger uncoupling between receptors and guanine nucleotide binding proteins. Herein we show that this kinase is subject to phosphorylation and regulation by protein kinase C (PKC). In cell lines stably expressing alpha1B- adrenergic receptors, activation of these receptors by epinephrine resulted in an activation of cytosolic betaARK. Similar data were obtained in 293 cells transiently coexpressing alpha1B- adrenergic receptors and betaARK-1. Direct activation of PKC with phorbol esters in these cells caused not only an activation of cytosolic betaARK-1 but also a translocation of betaARK immunoreactivity from the cytosol to the membrane fraction. A PKC preparation purified from rat brain phospborylated purified recombinant betaARK-1 to a stoichiometry of 0.86 phosphate per betaARK-1. This phosphorylation resulted in an increased activity of betaARK-1 when membrane-bound rhodopsin served as its substrate but in no increase of its activity toward a soluble peptide substrate. The site of phosphorylation was mapped to the C terminus of betaARK-1. We conclude that PKC activates betaARK by enhancing its translocation to the plasma membrane.
β - 肾上腺素能受体激酶(βARK)是胞质激酶家族的典型成员,该激酶可使鸟嘌呤核苷酸结合蛋白偶联受体磷酸化,从而引发受体与鸟嘌呤核苷酸结合蛋白之间的解偶联。在此我们表明,这种激酶会受到蛋白激酶C(PKC)的磷酸化作用和调控。在稳定表达α1B - 肾上腺素能受体的细胞系中,肾上腺素激活这些受体可导致胞质βARK的激活。在瞬时共表达α1B - 肾上腺素能受体和βARK - 1的293细胞中也获得了类似的数据。在这些细胞中用佛波酯直接激活PKC不仅会导致胞质βARK - 1的激活,还会使βARK免疫反应性从胞质转位至膜组分。从大鼠脑纯化的PKC制剂将纯化的重组βARK - 1磷酸化,磷酸化化学计量为每个βARK - 1有0.86个磷酸基团。当膜结合的视紫红质作为其底物时,这种磷酸化导致βARK - 1的活性增加,但对可溶性肽底物的活性没有增加。磷酸化位点定位于βARK - 1的C末端。我们得出结论,PKC通过增强βARK向质膜的转位来激活βARK。