农奴
磷化氢
内质网
化学
胞浆
钙
草酸盐
生物化学
钙ATP酶
基因亚型
网
生物物理学
ATP酶
细胞生物学
酶
生物
基因
有机化学
作者
Philip A. Bidwell,Evangelia G. Kranias
标识
DOI:10.1007/978-1-4939-3179-8_16
摘要
The various isoforms of the sarco/endoplasmic reticulum Ca(2+) ATPase (SERCA) are responsible for the Ca(2+) uptake from the cytosol into the endoplasmic or sarcoplasmic reticulum (ER/SR). In some tissues, the activity of SERCA can be modulated by binding partners, such as phospholamban and sarcolipin. The activity of SERCA can be characterized by its apparent affinity for Ca(2+) as well as maximal enzymatic velocity. Both parameters can be effectively determined by the protocol described here. Specifically, we describe the measurement of the rate of oxalate-facilitated (45)Ca uptake into the SR of crude mouse ventricular homogenates. This protocol can easily be adapted for different tissues and animal models as well as cultured cells.
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