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大鼠肝脏线粒体内膜的钙电导及钙电化学梯度的测定

The calcium conductance of the inner membrane of rat liver mitochondria and the determination of the calcium electrochemical gradient.

作者信息

Heaton G M, Nicholls D G

出版信息

Biochem J. 1976 Jun 15;156(3):635-46. doi: 10.1042/bj1560635.

Abstract
  1. A method is described for establishing steady-state conditions of calcium transport across the inner membrane of rat liver mitochondria and for determining the current of Ca2+ flowing across the membrane, together with the Ca2+ electrochemical gradient across the native Ca2+ carrier. These parameters were used to quantify the apparent Ca2+ conductance of the native carrier. 2. At 23 degrees C and pH7.0, the apparent Ca2+ conductance of the carrier is close to 1 nmol of Ca2+-min-1-mg of protein-1 mV-1. Proton extrusion by the respiratory chain, rather than the Ca2+ carrier itself, may often be rate-limiting in studies of initial rates of Ca2+ uptake. 3. Under parallel conditions, the endogenous H+ conductance of the membrane is 0.3 nmol of H+-min-1-mg of protein-1-mV-1. 4. Ruthenium Red and La3+ both strongly inhibit the Ca2+ conductance of the carrier, but are without effect on the H+ conductance of the membrane. 5. The apparent Ca2+ conductance of the carrier shows a sigmoidal dependence on the activity of Ca2+ in the medium. At 23 degrees C and pH7.2, half-maximum conductance is obtained at a Ca2+ activity of 4.7 muM. 6. The apparent Ca2+ conductance and the H+ conductance of the inner membrane increase fourfold from 23 degrees to 38 degrees C. The apparent Arrhenius activation energy for Ca2+ transport is 69kJ/mol. The H+ electrochemical gradient maintained in the absence of Ca2+ transport does not vary significantly with temperature. 7. The apparent Ca2+ conductance increases fivefold on increasing the pH of the medium from 6.8 to 8.0. The H+ conductance of the membrane does not vary significantly with pH over this range. 8. Mg2+ has no effect on the apparent Ca2+ conductance when added at concentration up to 1 mM. 9. Results are compared with classical methods of studying Ca2+ transport across the mitochondrial inner membrane.
摘要
  1. 本文描述了一种用于建立大鼠肝线粒体内膜钙转运稳态条件的方法,以及用于测定跨膜流动的Ca2+电流,同时测定跨天然Ca2+载体的Ca2+电化学梯度的方法。这些参数用于量化天然载体的表观Ca2+电导。2. 在23℃和pH7.0条件下,载体的表观Ca2+电导接近1 nmol Ca2+·min-1·mg蛋白-1·mV-1。在Ca2+摄取初始速率的研究中,呼吸链质子外排而非Ca2+载体本身通常可能是限速因素。3. 在平行条件下,膜的内源性H+电导为0.3 nmol H+·min-1·mg蛋白-1·mV-1。4. 钌红和La3+均强烈抑制载体的Ca2+电导,但对膜的H+电导无影响。5. 载体的表观Ca2+电导对介质中Ca2+活性呈S形依赖性。在23℃和pH7.2条件下,Ca2+活性为4.7μM时获得最大电导的一半。6. 内膜的表观Ca2+电导和H+电导在23℃至38℃范围内增加四倍。Ca2+转运的表观阿累尼乌斯活化能为69kJ/mol。在无Ca2+转运时维持的H+电化学梯度随温度变化不显著。7. 将介质pH从6.8提高到8.0时,表观Ca2+电导增加五倍。在此范围内,膜的H+电导随pH变化不显著。8. 当Mg2+浓度高达1 mM时,对表观Ca2+电导无影响。9. 将结果与研究线粒体内膜Ca2+转运的经典方法进行了比较。

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