Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/38791
Title: An Antibody Biosensor Establishes the Activation of the M1 Muscarinic Acetylcholine Receptor during Learning and Memory.
Authors: Butcher, Adrian J.
Bradley, Sophie J.
Prihandoko, Rudi
Brooke, Simon M.
Mogg, A.
Bourgognon, Julie-Myrtille
Macedo-Hatch, Timothy
Edwards, Jennifer M.
Bottrill, Andrew R.
Challiss, R. A. John
Broad, L. M.
Felder, C. C.
Tobin, Andrew B.
First Published: 29-Jan-2016
Publisher: American Society for Biochemistry and Molecular Biology
Citation: Journal of Biological Chemistry, 2016, 291 (17), pp. 8862-8875
Abstract: Establishing the in vivo activation status of G protein-coupled receptors would not only indicate physiological roles of G protein-coupled receptors but would also aid drug discovery by establishing drug/receptor engagement. Here, we develop a phospho-specific antibody-based biosensor to detect activation of the M1 muscarinic acetylcholine receptor (M1 mAChR) in vitro and in vivo Mass spectrometry phosphoproteomics identified 14 sites of phosphorylation on the M1 mAChR. Phospho-specific antibodies to four of these sites established that serine at position 228 (Ser(228)) on the M1 mAChR showed extremely low levels of basal phosphorylation that were significantly up-regulated by orthosteric agonist stimulation. In addition, the M1 mAChR-positive allosteric modulator, 1-(4-methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, enhanced acetylcholine-mediated phosphorylation at Ser(228) These data supported the hypothesis that phosphorylation at Ser(228) was an indicator of M1 mAChR activation. This was further supported in vivo by the identification of phosphorylated Ser(228) on the M1 mAChR in the hippocampus of mice following administration of the muscarinic ligands xanomeline and 1-(4-methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. Finally, Ser(228) phosphorylation was seen to increase in the CA1 region of the hippocampus following memory acquisition, a response that correlated closely with up-regulation of CA1 neuronal activity. Thus, determining the phosphorylation status of the M1 mAChR at Ser(228) not only provides a means of establishing receptor activation following drug treatment both in vitro and in vivo but also allows for the mapping of the activation status of the M1 mAChR in the hippocampus following memory acquisition thereby establishing a link between M1 mAChR activation and hippocampus-based memory and learning.
DOI Link: 10.1074/jbc.M115.681726
ISSN: 0021-9258
eISSN: 1083-351X
Links: http://www.jbc.org/content/291/17/8862
http://hdl.handle.net/2381/38791
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version free via Creative Commons CC-BY license.
Appears in Collections:Published Articles, Dept. of Molecular and Cell Biology

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