Schwartz G J, Lin J T, Kinne R
Anal Biochem. 1983 Feb 15;129(1):210-5. doi: 10.1016/0003-2697(83)90071-4.
A kinetic assay system which provides reliable measurements of Na-K-ATPase activity on 0.2 to 0.5-mm segments of renal proximal convoluted tubules isolated from collagenase-digested renal cortical slices is described. The use of collagenase digestion provides higher values for Na-K-ATPase, possibly by making the enzyme more accessible to the reaction system. The advantages of a kinetic vs an endpoint assay include the ability to use the same tubule as its own reference for the determination of total, ouabain-sensitive, and ouabain-insensitive ATPase activity. In addition, it allows dose-response studies on the effect of inhibitors on ATPase activity in the same tubule segment.
本文描述了一种动力学测定系统,该系统可对从胶原酶消化的肾皮质切片中分离出的0.2至0.5毫米肾近端曲管片段进行可靠的钠钾ATP酶活性测量。使用胶原酶消化可使钠钾ATP酶获得更高的值,这可能是因为使酶更容易与反应系统接触。动力学测定相对于终点测定的优势包括能够将同一肾小管作为自身对照,用于测定总ATP酶、哇巴因敏感型ATP酶和哇巴因不敏感型ATP酶的活性。此外,它还允许在同一肾小管片段上进行抑制剂对ATP酶活性影响的剂量反应研究。