Article (Scientific journals)
Measurement of plasma membrane calcium-calmodulin-dependent ATPase (PMCA) activity.
Mohamed, Tamer M. A.; Baudoin-Stanley, Florence M.; Abou-Leisa, Riham et al.
2010In Methods in Molecular Biology, 637, p. 333-42
Peer Reviewed verified by ORBi
 

Files


Full Text
book chapter 2010 pdf.pdf
Publisher postprint (613.74 kB)
Download

All documents in ORBilu are protected by a user license.

Send to



Details



Keywords :
Cell Line; Enzyme Assays/methods; Humans; Microsomes/metabolism; Plasma Membrane Calcium-Transporting ATPases/metabolism
Abstract :
[en] The plasma membrane calcium-calmodulin-dependent ATPase (PMCA) is a calcium-extruding enzymatic pump that ejects calcium from the cytoplasm to the extracellular compartment. Although in excitable cells such as skeletal and cardiac muscle cells PMCA has been shown to play only a minor role in regulating global intracellular calcium concentration, increasing evidence points to an important role for PMCA in signal transduction, in particular in the nitric oxide signaling pathway. Moreover, recent evidence has shown the functional importance of PMCA in mediating cardiac contractility and vascular tone. Here we describe a method in determining PMCA activity in the microsomal membrane preparation from cultured cells that overexpress specific isoform of PMCA by using modified coupled enzyme assay.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Mohamed, Tamer M. A.
Baudoin-Stanley, Florence M.
Abou-Leisa, Riham
Cartwright, Elizabeth
NEYSES, Ludwig ;  University of Luxembourg > Central Administration ; University of Luxembourg > Research Office
Oceandy, Delvac
External co-authors :
yes
Language :
English
Title :
Measurement of plasma membrane calcium-calmodulin-dependent ATPase (PMCA) activity.
Publication date :
2010
Journal title :
Methods in Molecular Biology
ISSN :
1064-3745
eISSN :
1940-6029
Publisher :
Humana Press, Clifton, United States - New Jersey
Volume :
637
Pages :
333-42
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 04 July 2016

Statistics


Number of views
68 (2 by Unilu)
Number of downloads
207 (4 by Unilu)

Scopus citations®
 
6
Scopus citations®
without self-citations
1
OpenCitations
 
7
OpenAlex citations
 
12

Bibliography


Similar publications



Contact ORBilu