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Preparation and functional characterization of a catalytically active fragment of phosphorylase kinase
Authors:Malencik  Dean A.  Zhao  Zhizhuang  Anderson  Sonia R.
Affiliation:(1) Department of Biochemistry and Biophysics, Oregon State University, 97331-7305 Corvallis, OR, USA;(2) Present address: Department of Biochemistry, University of Washington, 98195 Seattle, WA, USA
Abstract:Limited proteolysis of rabbit muscle phosphorylase kinase catalyzed by chymotrypsin generates a 33 kD product whose kinase activity is independent of both calcium and pH over the range of 6.8 to 8.3 (Malencik, D.A. & Fischer, E.H.Calcium and Cell Function III: 161–188, 1982). This active preparation consists of three related species containing residues 1–290, 1–296, and 1–298 of the 44.7 kD gamma-subunit of phosphorylase kinase (Harris, W.R., Malencik, D.A., Johnson, C.M., Carr, S.A., Roberts, G.D., Byles, C.E., Anderson, S.R., Heilmeyer, L.M.G., Fischer, E.H. & Crabb, J.W.J. Biol. Chem. 265:11740–11745, 1991). Good recoveries of catalytic activity — with varying degrees of calcium dependence — result upon the digestion of phosphorylase kinase with assorted proteases. However, especially high yields of the chymotryptic fragment are obtainable, with purification on an Ultrogel-34 column and a DEAE Sepharose CL-6B column giving 23% of the maximum possible protein.Physical characterization shows that the 33 kD chymotryptic fragment is globular, withs20,w=2.9S, and that it has an isoelectric point of 5.3. Our continuous catalytic assay, based on differences in the binding of the fluorescent dye 1-anilinonaphthalene-8-sulfonate by phosphorylasea andb, shows that, on a molar basis, the activity of the fragment is 2.8 fold greater than that of phosphorylase kinase (Malencik, D.A., Zhao, Z. and Anderson, S.R.Biochem. Biophys. Res. Comm. 174: 344–350, 1991). The active fragment also undergoes autophosphorylation. Incubation with Mg[gamma-P32] ATP results in the reaction of 0.7 mol32P/mol fragment. When the catalytic subunit of the cAMP-dependent protein kinase is also present, the amount of32P incorporated increases to 1.1 mol/mol. In the former case, phosphorylation occurs primarily at Ser30 while in the latter an additional reaction takes place at Ser81. The phosphopeptides correspond to sequences occurring in the gamma-subunit of phosphorylase kinase.Abbreviations cAMP adenosine 3(,5(-cyclic monophosphate - NaDodSO4 sodium dodecyl sulfate - Mops 3-(N-morpholino)propanesulfonic acid - Tris tris(hydroxymethyl)aminomethane - EDTA ethylenediaminetetraacetic acid - EGTA ethylene glycol bis(beta-aminoethyl ether)-N,N,N(,N(-tetraacetic acid - ANS 1-anilinonapththalene-8-sulfonate - TPCK N-tosyl phenylalanyl chloromethyl ketone - TLCK N-tosyllysyl chloromethyl ketone - PTH phenylthiohydantoinThe expected two to three fold increases in fluorescence intensity occur when assays are conducted with solutions containing 20 mM Tris chloride and no glycerophosphate.
Keywords:phosphorylase kinase  catalytic fragment of   /content/h1471571w220505n/xxlarge947.gif"   alt="  gamma"   align="  MIDDLE"   BORDER="  0"  >-subunit  phosphorylation of phosphorylase kinase  fluorometric assay
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