首页> 外文期刊>Biophysical Chemistry: An International Journal Devoted to the Physical Chemistry of Biological Phenomena >An improved approximate solution of the Lamm equation for the simultaneous estimation of sedimentation and diffusion coefficients from sedimentation velocity experiments
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An improved approximate solution of the Lamm equation for the simultaneous estimation of sedimentation and diffusion coefficients from sedimentation velocity experiments

机译:Lamm方程的改进近似解,可同时通过沉降速度实验估算沉降和扩散系数

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摘要

Sedimentation and diffusion coefficients are important parameters to describe size and shape of macromolecules in solution. The data can be obtained from sedimentation velocity experiments by a nonlinear fitting procedure using approximate solutions for the Lamm equation. Here, we present a modification of such a model function that was originally proposed by Fujita [H. Fujita, Mathematical Theory of Sedimentation Analysis, Wiley, New York, 1962]. The extended model function is well suitable to study low molecular mass compounds. The improvement of this solution given here is based on using an adjustable value for the explicit integration variable, z, the reduced radius. This modification leads to more accurate sedimentation and diffusion coefficients compared to using a constant value of 0.5 as used by Fujita. The advantage of our modification was demonstrated by the analysis of noise-free curves calculated using the finite element method, as well as experimental curves obtained for the peptides angiotensin I and II. The relatively low sedimentation and diffusion coefficients found for both substances indicate that the peptides exist as extended chains of about 3.65 nm (angiotensin I) or 3.04 nm length (angiotensin II) in solution. The lack of higher-order structure of the peptides that was derived also from CD spectra might facilitate receptor binding, and could be one reason for the fast proteolytic digestion of the free peptides. (C) 1998 Elsevier Science B.V. [References: 23]
机译:沉积和扩散系数是描述溶液中大分子的大小和形状的重要参数。可以通过使用Lamm方程的近似解的非线性拟合程序从沉降速度实验中获得数据。在这里,我们介绍了藤田[H.藤田,沉积分析的数学理论,威利,纽约,1962年]。扩展的模型函数非常适合研究低分子量化合物。此处给出的此解决方案的改进基于对显式积分变量z(减小的半径)使用可调值。与使用Fujita使用的常数0.5相比,此修改导致更精确的沉降和扩散系数。通过分析使用有限元方法计算出的无噪声曲线以及获得的血管紧张素I和II肽的实验曲线,证明了我们修饰的优势。两种物质的相对较低的沉降和扩散系数表明,肽在溶液中以约3.65 nm(血管紧张素I)或3.04 nm长(血管紧张素II)的延伸链存在。缺乏也来源于CD光谱的肽的高阶结构可能会促进受体结合,并且可能是游离肽快速蛋白水解消化的原因之一。 (C)1998 Elsevier Science B.V. [参考:23]

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