Literature DB >> 23007597

Measurement of Ca²⁺-ATPase activity (in PMCA and SERCA1).

Danuta Kosk-Kosicka1.   

Abstract

Ca(2+)-ATP pumps (those on the plasma membrane; PMCA and sarcoplasmic reticulum; SERCA1) have an important role to play in the regulation of intracellular calcium concentrations. In this chapter, three preparations, two membranes and a purified enzyme, best suited for studies of Ca(2+)-ATPase activity are described. The two selected membranes are the human red blood cell (RBC) ghosts, a representative of plasma membranes (PM), and the rabbit skeletal muscle SR, an intracellular membrane. In this protocol, Pi released during the ATPase reaction is subsequently measured colorimetrically as a complex of molybdovanadate. The method is simple (one-step), fast, sensitive, and reliable.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23007597     DOI: 10.1007/978-1-62703-086-1_21

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Interactions between small ankyrin 1 and sarcolipin coordinately regulate activity of the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1).

Authors:  Patrick F Desmond; Amanda Labuza; Joaquin Muriel; Michele L Markwardt; Allison E Mancini; Mark A Rizzo; Robert J Bloch
Journal:  J Biol Chem       Date:  2017-05-09       Impact factor: 5.157

2.  Identification of Small Ankyrin 1 as a Novel Sarco(endo)plasmic Reticulum Ca2+-ATPase 1 (SERCA1) Regulatory Protein in Skeletal Muscle.

Authors:  Patrick F Desmond; Joaquin Muriel; Michele L Markwardt; Mark A Rizzo; Robert J Bloch
Journal:  J Biol Chem       Date:  2015-09-24       Impact factor: 5.157

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.