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Straightforward and rapid method for detection of cyclin-dependent kinase-like 5 activity
- Source :
- Analytical biochemistry. 566
- Publication Year :
- 2018
-
Abstract
- Cyclin-dependent kinase-like 5 (CDKL5) is a serine/threonine protein kinase, with its gene mutation leading to a neurodevelopmental disorder. Pathogenic point mutations are mostly observed within the catalytic domain of CDKL5, therefore loss of catalytic activity may be related to disease onset. However, this hypothesis has rarely been demonstrated. Here, we report an efficient method for detecting CDKL5 activity. Appropriately, CDKL5 underwent autophosphorylation following expression in Escherichia coli, with autophosphorylated CDKL5 detected as a band shift by phos-tag SDS–PAGE, without enzyme purification. Thus, this protocol is useful for examining the relationship between disease-causing mutations and their activity.
- Subjects :
- Biophysics
CDKL5
Mutation, Missense
Gene mutation
Protein Serine-Threonine Kinases
01 natural sciences
Biochemistry
Serine
03 medical and health sciences
Cyclin-dependent kinase
Catalytic Domain
Escherichia coli
Threonine
Cloning, Molecular
Phosphorylation
Protein kinase A
Molecular Biology
030304 developmental biology
Enzyme Assays
0303 health sciences
biology
Chemistry
Point mutation
010401 analytical chemistry
Autophosphorylation
Cell Biology
Molecular biology
0104 chemical sciences
biology.protein
Subjects
Details
- ISSN :
- 10960309
- Volume :
- 566
- Database :
- OpenAIRE
- Journal :
- Analytical biochemistry
- Accession number :
- edsair.doi.dedup.....6aa2a1cc398a1753e21b43fb44a5716c