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

Welsh, Gavin I., Patel, Jashmin, Proud, Christopher G. (1997) Peptide substrates suitable for assaying glycogen synthase kinase-3 in crude cell extracts. Analytical Biochemistry, 244 (1). pp. 16-21. ISSN 0003-2697. (doi:10.1006/abio.1996.9838) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:18037)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
http://dx.doi.org/10.1006/abio.1996.9838

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. (C) 1997 Academic Press, Inc.

Item Type: Article
DOI/Identification number: 10.1006/abio.1996.9838
Subjects: Q Science > QD Chemistry
Divisions: Divisions > Division of Natural Sciences > Biosciences
Depositing User: T.J. Sango
Date Deposited: 29 Apr 2009 13:02 UTC
Last Modified: 05 Nov 2024 09:53 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/18037 (The current URI for this page, for reference purposes)

University of Kent Author Information

Proud, Christopher G..

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