Kurganov B I
Bakh Institute of Biochemistry, Russian Academy of Sciences, Leninskii pr. 33, Moscow, 117071 Russia.
Biochemistry (Mosc). 1998 Mar;63(3):364-6.
The mechanism of heat aggregation of proteins proposed by the author involves the stage of irreversible denaturation, the stage of nucleation, and the stage of growth of aggregates. It was shown that the initial parts of the kinetic curves of aggregation followed by monitoring the increase in absorbance (A) or intensity of light scattering (I) are linearized in coordinates (dA/dt; t) and (A; t2) (or, respectively, in coordinates (dI/dt; t) and (I; t2)). The slope of these linear anamorphoses is proportional to the product of the rate constant of irreversible denaturation and the rate constant of growth of aggregates. The mechanism of heat aggregation proposed is fulfilled for pig heart citrate synthase. The dI/dt versus t curves for heat aggregation of glycogen phosphorylase b from rabbit skeletal muscles display a lag period whose appearance is caused by intramolecular predenaturational changes in the enzyme molecule.
作者提出的蛋白质热聚集机制涉及不可逆变性阶段、成核阶段和聚集体生长阶段。结果表明,通过监测吸光度(A)或光散射强度(I)的增加来跟踪聚集动力学曲线的初始部分,在坐标(dA/dt;t)和(A;t2)(或者分别在坐标(dI/dt;t)和(I;t2))中呈线性关系。这些线性变形的斜率与不可逆变性速率常数和聚集体生长速率常数的乘积成正比。所提出的热聚集机制适用于猪心柠檬酸合酶。兔骨骼肌糖原磷酸化酶b热聚集的dI/dt与t曲线显示出一个延迟期,其出现是由酶分子内的分子内预变性变化引起的。