Stimulation of liver glycogen particle synthase D phosphatase activity by caffeine, AMP, and glucose 6-phosphate

Daniel P. Gilboe, Frank Q. Nuttall

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30 Scopus citations

Abstract

Caffeine stimulates synthase and phosphorylase phosphatase activities by independent mechanisms. Both effects of caffeine are concentration-dependent with different apparent A0.5 for each reaction. Stimulation of the synthase phosphatase reaction was independent of the initial phosphorylase a concentration, was immediate, and did not follow in sequence the depletion of phosphorylase a. Glucose 6-phosphate also was stimulatory to the synthase phosphatase reaction (A0.5 = 0.14 mM) with little effect on phosphorylase phosphatase. In combination glucose 6-phosphate and caffeine effects were additive suggesting the existence of separate binding sites. The synthase phosphatase reaction also was stimulated by AMP (binding affinity 2.3 mm) but with no effect on phosphorylase phosphatase activity. Together caffeine and AMP effects were not additive suggesting that they share a common binding site or closely interrelated sites. The location of the AMP and caffeine site(s) has not yet been determined.

Original languageEnglish (US)
Pages (from-to)179-185
Number of pages7
JournalArchives of Biochemistry and Biophysics
Volume219
Issue number1
DOIs
StatePublished - Nov 1982

Bibliographical note

Funding Information:
The authors gratefully acknowledge the excellect technical assistance of Ms. Diane Miller and Ms. Jane Gillette. This study was supported with research funds provided by the Veterans Administration.

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