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Structure determination of asymmetric membrane profiles using an iterative Fourier method.

机译:使用迭代傅里叶方法确定不对称膜轮廓的结构。

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摘要

An iterative Fourier method is applied to solving and refining the electron density profile projected into the line perpendicular to a membrane surface. Solutions to the continuous X-ray scattering pattern derived from swelling of multilayer systems or from membrane dispersions can be obtained by this technique. The method deals directly with the observed structure factors and does not rely on deconvolution of the Patterson function. We used this method previously to derive the electron density profile for acetylcholine receptor membranes (Ross et al., 1977). The present paper is an analysis of the theoretical basis for the procedure. In addition, the technique is tested on artificially generated continuous-scattering data, on the data for frog sciatic nerve myelin derived from swelling experiments by Worthington and McIntosh (1974), and on the data for purple membrane (Blaurock and Stoeckenius, 1971). Although the method applies to asymmetric membranes, the special case of centrosymmetric profiles is also shown to be solvable by the same technique. The limitations of the method and the boundary conditions that limit the degeneracy of the solution are analyzed.
机译:迭代傅里叶方法用于求解和改进投射到垂直于膜表面的直线中的电子密度分布。可以通过该技术获得源自多层系统的溶胀或源自膜分散体的连续X射线散射图案的解决方案。该方法直接处理观察到的结构因素,而不依赖于Patterson函数的反卷积。我们以前使用这种方法来推导乙酰胆碱受体膜的电子密度分布(Ross等,1977)。本文是对该程序的理论基础的分析。此外,该技术还通过人工生成的连续散射数据,沃辛顿和麦金托什(1974)的溶胀实验得到的青蛙坐骨神经髓鞘数据以及紫色膜的数据进行了测试(Blaurock和Stoeckenius,1971)。尽管该方法适用于不对称膜,但中心对称轮廓的特殊情况也显示可以通过相同技术解决。分析了该方法的局限性和限制解的简并性的边界条件。

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