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首页> 外文期刊>The Journal of Physiology >Effect of temperature on elementary steps of the cross-bridge cycle in rabbit soleus slow-twitch muscle fibres.
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Effect of temperature on elementary steps of the cross-bridge cycle in rabbit soleus slow-twitch muscle fibres.

机译:温度对兔比目鱼慢肌肌肉纤维中跨桥循环基本步骤的影响。

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1. Isometric tension, stiffness and the cross-bridge kinetics in rabbit soleus slow-twitch fibres (STFs) were studied in the temperature range 5-37 degrees C by sinusoidal analysis. 2. The effects of MgATP and phosphate (Pi) on the cross-bridge kinetics were studied, and the temperature dependence of the kinetic constants of elementary steps of the cross-bridge cycle was deduced in the range 20-37 degrees C. 3. The MgATP association constant (K1a) decreased when temperature was increased. The rate constants of the ATP-isomerization step (k1b and k-1b) and the cross-bridge detachment step (k2, and k(-2)) had Q10 values of 3-4, and hence their equilibrium constants (K1b and K2) changed little with temperature. 4. Q10 of the force generation step (k4) was the largest at 6.7; its reversal step (k(-4)) had a Q10 of 2.5, and hence its equilibrium constant (K4) increased significantly with temperature. The Pi association constant (K5) changed little with temperature. 5. The elementary steps of the cross-bridge cycle are more temperature sensitive in soleus STFs than in psoas, which are fast-twitch fibres. This is in accord with a higher temperature sensitivity of the apparent rate constants in STFs.T 6. The temperature dependence of the equilibrium constant of the force generation step (K4) was fitted to the modified Van't Hoff equation to deduce standard enthalpy change (DeltaH degrees; 70 +/- 20 kJ mol(-1)), standard entropy change (DeltaS degrees; 250 +/- 70 J mol(-1) K(-1)), and heat capacity change (DeltaCp; -12 +/- 5 kJ mol(-1) K(-1)). These results indicate that the force generation step is an entropy driven, endothermic reaction that accompanies a burial of large surface area. These observations are consistent with the hypothesis that hydrophobic interaction between residues of actin and myosin and between residues of the myosin head underlies the mechanism of force generation. 7. An increase of isometric tension with temperature is accounted for by the increased number of cross-bridges in tension generating states. Stiffness also increased with temperature, but to a lesser degree.
机译:1.通过正弦分析研究了在比目鱼比目鱼慢弹力纤维(STFs)在5-37摄氏度的温度范围内的等轴测张力,刚度和跨桥动力学。 2.研究了MgATP和磷酸盐(Pi)对跨桥动力学的影响,并推导了跨桥循环基本步骤动力学常数的温度依赖性在20-37摄氏度范围内。3。当温度升高时,MgATP缔合常数(K1a)降低。 ATP异构化步骤(k1b和k-1b)和跨桥分离步骤(k2和k(-2))的速率常数的Q10值为3-4,因此它们的平衡常数(K1b和K2 )随温度变化不大。 4.力生成步骤(k4)的Q10最大,为6.7;它的逆转步骤(k(-4))的Q10为2.5,因此其平衡常数(K4)随温度显着增加。 Pi关联常数(K5)随温度变化很小。 5.比目鱼STFs比快肌纤维腰大肌对跨桥循环的基本步骤对温度更敏感。这符合STFs中表观速率常数的较高温度敏感性。T6.将力生成步骤(K4)的平衡常数的温度依赖性拟合到修改后的Van't Hoff方程中,以推导出标准焓变。 (DeltaH度; 70 +/- 20 kJ mol(-1)),标准熵变(DeltaS度; 250 +/- 70 J mol(-1)K(-1))和热容变化(DeltaCp;- 12 +/- 5 kJ mol(-1)K(-1))。这些结果表明,力产生步骤是熵驱动的吸热反应,伴随着大表面积的埋葬。这些观察结果与肌动蛋白和肌球蛋白残基之间以及肌球蛋白头部的残基之间的疏水相互作用是力产生机理的基础的假设相一致。 7.等轴测张力随温度的增加是由于张力产生状态下横桥数量的增加所致。刚度也随温度而增加,但程度较小。

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