An assay of human tyrosine protein kinase ABL activity using an Escherichia coli protein expression system

ABL, a human tyrosine protein kinase, and its substrate are co-expressed in Escherichia coli. Tyrosine phosphorylation of the substrate in E. coli was detected using Phos-tag SDS-PAGE. The bacterial co-expression system was used as a field for the kinase reaction to evaluate the enzymatic activity o...

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Veröffentlicht in:BioTechniques. - 1993. - 70(2021), 4 vom: 01. Apr., Seite 209-217
1. Verfasser: Kinoshita-Kikuta, Emiko (VerfasserIn)
Weitere Verfasser: Yoshimoto, Momoka, Yano, Marina, Kinoshita, Eiji, Koike, Tohru
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2021
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Journal Article Research Support, Non-U.S. Gov't ABL Escherichia coli abltide co-expression phos-tag tyrosine protein kinase Escherichia coli Proteins Pyrimidines mehr... Imatinib Mesylate 8A1O1M485B Fusion Proteins, bcr-abl EC 2.7.10.2
Beschreibung
Zusammenfassung:ABL, a human tyrosine protein kinase, and its substrate are co-expressed in Escherichia coli. Tyrosine phosphorylation of the substrate in E. coli was detected using Phos-tag SDS-PAGE. The bacterial co-expression system was used as a field for the kinase reaction to evaluate the enzymatic activity of five types of ABL kinase domain mutants. Relative to wild-type ABL, kinase activity was comparable in the H396P mutant, reduced in both Y253F and E255K mutants and undetectable in T315I and M351T mutants. These comparative results demonstrated that the phosphorylation states of the mutants correlated with their activity. The bacterial co-expression system permits rapid production of tyrosine kinase variants and provides a simple approach for examining their structure-activity relationships
Beschreibung:Date Completed 20.12.2021
Date Revised 20.12.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1940-9818
DOI:10.2144/btn-2020-0154