Literature DB >> 9025901

Peptide substrates suitable for assaying glycogen synthase kinase-3 in crude cell extracts.

G I Welsh1, J C Patel, C G Proud.   

Abstract

In this study we describe the characterization and use of new peptide substrates for assaying glycogen synthase kinase-3 (GSK-3) which are based on the sequence around the single GSK-3 phosphorylation site in the translation factor eIF2B. The new peptides offer important advantages over previous substrates, which were based on the sequence around the multiple GSK-3 phosphorylation sites in glycogen synthase (GS), for the assay of GSK-3 in cell extracts. In particular, decreases in GSK-3 activity following, e.g., insulin treatment, are partially or completely masked when the GS-based peptides are used but are readily measured using the new, eIF2B-based, peptides. The new peptides, unlike those based on GS, are therefore suitable for the assay of changes in GSK-3 activity in cell extracts without the need for prior immunoprecipitation or ion-exchange chromatography.

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Year:  1997        PMID: 9025901     DOI: 10.1006/abio.1996.9838

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  14 in total

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Authors:  C G Proud; R M Denton
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5.  Nutrients differentially regulate multiple translation factors and their control by insulin.

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9.  Selective enhancement of the uptake and bioactivity of a TAT-conjugated peptide inhibitor of glycogen synthase kinase-3.

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Journal:  Mol Ther       Date:  2008-12-23       Impact factor: 11.454

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