Electrochemical studies of human nAChR a7 subunit phosphorylation by kinases PKA, PKC and Src.
Electrochemistry
Enzyme
Kinetics
Nicotinic acetylcholine receptors
Phosphorylation
XPS
Journal
Analytical biochemistry
ISSN: 1096-0309
Titre abrégé: Anal Biochem
Pays: United States
ID NLM: 0370535
Informations de publication
Date de publication:
01 06 2019
01 06 2019
Historique:
received:
09
01
2019
revised:
19
03
2019
accepted:
19
03
2019
pubmed:
28
3
2019
medline:
18
2
2020
entrez:
28
3
2019
Statut:
ppublish
Résumé
Nicotinic acetylcholine receptors (nAChR) are ion channels which regulate a numerous of neurotransmitters, including acetylcholine, norepinephrine, dopamine, serotonin and glutamate. These receptors are important targets for the study of a plethora of diseases such as Alzheimer's disease, schizophrenia, Parkinson's Disease, cancer, inflammation, etc. The α7 subunits are especially interesting in that they are commonly occurring and are critical sites of regulation. Herein we report the phosphorylation of the human nAChR α7 subunits, by the kinases PKA, PKC and Src, by both biochemical and electrochemical techniques along with the kinetics of each phosphorylation reaction. Phosphorylation was investigated through changes in current density as well as impedance and X-ray photo electron spectroscopy (XPS) and the kinetics were determined electrochemically using the surface Michaelis-Menten model. Our results clearly demonstrate the phosphorylation of the nAChR α7 and the invaluable strength of surface electrochemical techniques in the investigation of protein phosphorylation.
Identifiants
pubmed: 30914244
pii: S0003-2697(19)30035-1
doi: 10.1016/j.ab.2019.03.012
pii:
doi:
Substances chimiques
alpha7 Nicotinic Acetylcholine Receptor
0
src-Family Kinases
EC 2.7.10.2
Cyclic AMP-Dependent Protein Kinases
EC 2.7.11.11
Protein Kinase C
EC 2.7.11.13
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
46-56Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.