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  5. Quantifying the Kinase Activities of MST1/2
 
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Quantifying the Kinase Activities of MST1/2

Author(s)
O'Driscoll, Niamh A.  
Matallanas, David  
Uri
http://hdl.handle.net/10197/9877
Date Issued
2018-12-19
Date Available
2019-04-10T08:58:49Z
Abstract
The functions of the kinases MST1 and MST2 rely heavily on their ability to phosphorylate and become phosphorylated themselves. Hence, it is important to precisely measure the kinase activities of both isoforms in a reproducible manner. Here, we describe in detail the protocol for an in-gel kinase assay for the quantification of the kinase activity of MST1/2, which involves immunoprecipitation of MST1/2 and the incorporation of radiolabeled phosphate from [γ-32P]-ATP into a substrate immobilized in a polyacrylamide gel. We also include a protocol for indirect measurement of MST1/2 activation status using immunoblotting.
Sponsorship
Science Foundation Ireland
Type of Material
Book Chapter
Publisher
Springer
Series
Methods in Molecular Biology
Volume: 1893
Copyright (Published Version)
2019 Springer Nature
Subjects

Immunoprecipitation

Kinase assay

MST1

MST2

Radiolabel

DOI
10.1007/978-1-4939-8910-2_22
Language
English
Status of Item
Peer reviewed
Journal
Hergovich, A. (ed.). The Hippo Pathway. Methods in Molecular Biology
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by-nc-nd/3.0/ie/
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Chapter 27_Quantifying the kinase activities of MST1 MiMB O'Driscoll_editor feedback_Author revisions..docx

Size

72.04 KB

Format

Unknown

Checksum (MD5)

d5c18a00c786f7d3dc8deda8b817db3c

Owning collection
Medicine Research Collection

Item descriptive metadata is released under a CC-0 (public domain) license: https://creativecommons.org/public-domain/cc0/.
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