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PMID: 8117294 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Design and synthesis of two new peptide substrates for the specific and sensitive monitoring of casein kinases-1 and -2.

Biochemical and biophysical research communications ·Vol. 198 ·No. 3 ·1994-02-15 ·Pages 898-905

Marin O, Meggio F, Pinna LA

Abstract

The available information about the specificity determinants of casein kinases-1 and -2 (CK1 and CK2) has been utilized to obtain two new peptide substrates optimally suited for the specific monitoring of these two pleiotropic enzymes. The best substrate developed for CK1 is the inhibitor-2 derived peptide RRKDLHDDEEDEAMSITA which is superior in every respect to all the non phosphorylated CK1 peptide substrates used so far. Its Km is 172 microM and the Vmax is 6-fold higher than that of casein. The dodecapeptide RRRADDSDDDDD, on the other hand, is totally refractory to CK1 while it is an excellent substrate for CK2, exhibiting, under basal conditions, a Km value of 19 microM and a Vmax higher than those obtained with all the routinely used substrates of CK2. Both the novel CK1 and CK2 peptide substrates are suited for the phosphocellulose paper assay.

MeSH Terms
Amino Acid Sequence Casein Kinases Indicators and Reagents Isoenzymes/analysis,metabolism Kinetics Molecular Sequence Data Oligopeptides/chemical synthesis,metabolism Peptides/chemical synthesis,metabolism Phosphorylation Protein Kinases/analysis,metabolism Substrate Specificity
Chemicals
Indicators and Reagents Isoenzymes Oligopeptides Peptides Protein Kinases Casein Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Marin O
Dipartimento di Chimica Biologica, CRIBI and CNR, Università di Padova, Italy.
Meggio F
Pinna L A
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1994-02-15
Pages
898-905
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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