Characterization of 5′-AMP-Activated Protein Kinase in Human Liver Using Specific Peptide Substrates and the Effects of 5′-AMP Analogues on Enzyme Activity

A specific peptide (SAMS peptide) phosphorylation assay has previously been used to measure and subsequently purify rat liver 5′-AMP-activated protein kinase (AMPK). In this report, we show that this peptide and a peptide based on the sequence surrounding the site phosphorylated on 3-hydroxy-3-methy...

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Veröffentlicht in:Biochemical and biophysical research communications 1994-05, Vol.200 (3), p.1551-1556
Hauptverfasser: Sullivan, J.E., Carey, F., Carling, D., Beri, R.K.
Format: Artikel
Sprache:eng
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Zusammenfassung:A specific peptide (SAMS peptide) phosphorylation assay has previously been used to measure and subsequently purify rat liver 5′-AMP-activated protein kinase (AMPK). In this report, we show that this peptide and a peptide based on the sequence surrounding the site phosphorylated on 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase by AMPK (HMG peptide) can be used to measure human liver AMPK. Our data demonstrate that both human and rat AMPKs have a higher affinity for the HMG peptide compared to the SAMS peptide. We have used these peptide phosphorylation assays to identify novel activators of AMPK.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.1994.1627