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通过测量[³H]哇巴因结合来完全定量大鼠骨骼肌钠钾依赖ATP酶的总浓度。

Complete quantification of the total concentration of rat skeletal-muscle Na+ + K+-dependent ATPase by measurements of [3H]ouabain binding.

作者信息

Kjeldsen K

出版信息

Biochem J. 1986 Dec 15;240(3):725-30. doi: 10.1042/bj2400725.

Abstract

In the standard [3H]ouabain-binding assay for quantification of the Na,K-ATPase (Na+ + K+-dependent ATPase) concentration in rat skeletal muscles, samples are incubated for 2 X 60 min in 1 microM-[3H]ouabain at 37 degrees C followed by a wash-out for 4 X 30 min at 0 degree C. To obtain accurate determinations, values determined by this standard assay should be corrected for non-specific uptake and retention of [3H]ouabain (11% overestimation), loss of specifically bound [3H]ouabain during wash-out (21% underestimation), evaporation from muscle samples during weighing (4% overestimation), impurity of [3H]ouabain (5% underestimation) and incomplete saturation of [3H]ouabain binding sites (6% underestimation). Thus corrected the standard [3H]ouabain-binding assay determines the total Na,K-ATPase concentration. Hence, in the soleus muscle of 12-week-old rats the total [3H]ouabain-binding-site concentration is 278 +/- 20 pmol/g wet wt. This is at variance with the evaluation of the Na,K-ATPase concentration from Na,K-ATPase activity measurements in muscle membrane fractions, where the recovery of Na,K-ATPase is only 2-18%. Quantification of the total Na,K-ATPase concentration is of particular importance since it is a prerequisite for the discussion of quantitative aspects of the Na,K-ATPase.

摘要

在用于定量大鼠骨骼肌中钠钾 - ATP酶(Na⁺ + K⁺依赖性ATP酶)浓度的标准[³H]哇巴因结合试验中,将样品在37℃下于1微摩尔[³H]哇巴因中孵育2×60分钟,随后在0℃下洗脱4×30分钟。为了获得准确的测定结果,通过该标准试验测定的值应针对[³H]哇巴因的非特异性摄取和保留(高估11%)、洗脱过程中特异性结合的[³H]哇巴因的损失(低估21%)、称重期间肌肉样品的蒸发(高估4%)、[³H]哇巴因的杂质(低估5%)以及[³H]哇巴因结合位点的不完全饱和(低估6%)进行校正。经过这样校正后,标准[³H]哇巴因结合试验可测定总钠钾 - ATP酶浓度。因此,在12周龄大鼠的比目鱼肌中,总[³H]哇巴因结合位点浓度为278±20皮摩尔/克湿重。这与通过肌肉膜组分中钠钾 - ATP酶活性测量评估钠钾 - ATP酶浓度的结果不同,在后者中钠钾 - ATP酶的回收率仅为2 - 18%。总钠钾 - ATP酶浓度的定量尤为重要,因为它是讨论钠钾 - ATP酶定量方面的前提条件。

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