L.U.R.E. Bâtiment 209c, Université Paris-Sud, F-91405 Orsay Cedex, France.
EMBO J. 1982;1(1):35-40. doi: 10.1002/j.1460-2075.1982.tb01120.x.
Structural models of biological macromolecules can be tested by comparing calculated and experimental solution scattering curves. We have developed an approach for computing scattering shape functions at medium resolution from models proposed on the basis of other techniques such as electron microscopy. We present the results obtained with the 50S ribosomal subunit from Escherichia coli; two models are considered, one proposed by Lake (1976), the other one by Tischendorf et al. (1975). Although the two models are similar in many respects, their scattering shape functions are significantly different. The comparison with the experimental scattering curve allows us to check the scale of the models and, after scaling, to quantitate the agreement between the observed and the calculated curves. Finally, it can provide a starting point for the structural interpretation of the X-ray data.
生物大分子的结构模型可以通过比较计算和实验溶液散射曲线来进行测试。我们已经开发了一种从中介分辨率的模型(例如电子显微镜)计算散射形状函数的方法。我们给出了来自大肠杆菌 50S 核糖体亚基的结果;考虑了两种模型,一种是由 Lake(1976)提出的,另一种是由 Tischendorf 等人(1975)提出的。尽管这两种模型在许多方面相似,但它们的散射形状函数却有很大的不同。与实验散射曲线的比较可以检查模型的比例,并且在缩放之后,可以量化观察到的和计算出的曲线之间的一致性。最后,它可以为 X 射线数据的结构解释提供起点。