Zipper P, Durchschlag H
Z Naturforsch C Biosci. 1980 Nov-Dec;35(11-12):890-901. doi: 10.1515/znc-1980-11-1204.
Malate synthase undergoes an X-ray induced aggregation which can be monitored in situ by small-angle X-ray scattering; the analysis of scattering curves, taken at subsequent stages of aggregation, has led to the establishment of a tentative model for an aggregation in two dimensions (Zipper and Durchschlag (1980) Rad. and Environm. Biophys., in press). This model was checked by comparison of appropriate theoretical curves with the experimental curves. The theoretical scattering curves for this comparison were obtained by weighted averaging over the scattering curves calculated for various species of hypothetical aggregates. Based on the approximation of the unaggregated enzyme particle by an oblate cylinder, the aggregates were assumed to be composed of 2, 3, 4 or 6 of such cylinders, associated side-by-side in one and later on in two linear rows. THe weight fractions of the species were chosen so, that an optimum fit of the experimental mean radii of gyration and mean degrees of aggregation was achieved. The distance distribution functions calculated for the model are very similar to the functions derived from the scattering experiment. Cross-section Guinier plots of the scattering curves of the model reveal the occurrence of one and later on of two pseudo cross-section factors similar to those observed in the experimental scattering curves. The pseudo thickness factor of the model of the unaggregated particle is found to be retained in the model curves for all stages of aggregation. From these results it can be concluded that the model for the aggregation process is essentially consistent with the scattering behaviour of the aggregating enzyme. Small differences between the theoretical and experimental curves may be explained by the idealizations of the model. The comparison of theoretical curves for alternative models, assuming aggregation in three dimensions, suggests that these models are unlikely, though small amounts of three-dimensional aggregates cannot be ruled out completely.
苹果酸合酶会发生X射线诱导的聚集,这可以通过小角X射线散射原位监测;对聚集后续阶段所取散射曲线的分析,已得出二维聚集的初步模型(齐珀和杜尔施拉格(1980年),《辐射与环境生物物理学》,即将发表)。通过将适当的理论曲线与实验曲线进行比较来检验该模型。用于此比较的理论散射曲线是通过对为各种假设聚集体物种计算的散射曲线进行加权平均得到的。基于用扁圆柱近似未聚集的酶颗粒,假定聚集体由2、3、4或6个这样的圆柱组成,先是并排关联成一排,随后是两排直线排列。选择这些物种的重量分数,以便实现实验回转半径平均值和聚集平均程度的最佳拟合。为该模型计算的距离分布函数与从散射实验得出的函数非常相似。该模型散射曲线的横截面吉尼尔图显示,出现了一个以及随后两个类似于在实验散射曲线中观察到的伪横截面因子。发现未聚集颗粒模型的伪厚度因子在聚集的所有阶段的模型曲线中都得以保留。从这些结果可以得出结论,聚集过程的模型与聚集酶的散射行为基本一致。理论曲线与实验曲线之间的小差异可能由模型的理想化来解释。对假设三维聚集的替代模型的理论曲线进行比较表明,这些模型不太可能,尽管不能完全排除少量三维聚集体的存在。