Burghardt T P, Thompson N L
Biophys J. 1985 Sep;48(3):401-9. doi: 10.1016/S0006-3495(85)83796-6.
A model-independent description of the angular orientation distribution of elements in an ordered biological assembly is applied to the electron spin resonance (ESR) technique. As in a previous model-independent treatment of fluorescence polarization (Burghardt, T.P., 1984, Biopolymers, 23:2383-2406) the elemental order is described by an angular distribution of molecular frames with one frame fixed in each element of the assembly. The distribution is expanded in a complete orthonormal set of functions. The coefficients of the series expansion (the order parameters) describe the orientation distribution of the elements in the assembly without reference to a model and can be obtained from the observed spectrum. The method establishes the limitations of ESR in detecting order in the assembly by determining which distribution coefficients the technique can detect. A method of determining the order parameters from an ESR spectra, using a set of ESR basis spectra, is developed. We also describe a treatment that incorporates the actual line shape measured from randomly oriented, immobile elements. In this treatment, no model-dependent assumptions about the line shape are required. We have applied the model-independent analysis to ESR spectra from spin-labeled myosin cross-bridges in muscle fibers. The results contain detailed information on the spin-probe angular distribution and differ in interesting ways from previous model-dependent interpretations of the spectra.
一种与模型无关的对有序生物组装体中元素角取向分布的描述被应用于电子自旋共振(ESR)技术。如同之前对荧光偏振进行的与模型无关的处理(Burghardt, T.P., 1984,《生物聚合物》, 23:2383 - 2406),元素顺序由分子框架的角分布来描述,其中每个框架在组装体的每个元素中固定。该分布在一组完备的正交归一函数集中展开。级数展开的系数(序参量)描述了组装体中元素的取向分布,无需参考模型,并且可以从观测光谱中获得。该方法通过确定该技术能够检测哪些分布系数来确定ESR在检测组装体中顺序方面的局限性。开发了一种使用一组ESR基谱从ESR光谱确定序参量的方法。我们还描述了一种纳入从随机取向的固定元素测量的实际线形的处理方法。在这种处理中,不需要对线形做与模型相关的假设。我们已将这种与模型无关的分析应用于肌肉纤维中自旋标记肌球蛋白横桥的ESR光谱。结果包含有关自旋探针角分布的详细信息,并且在有趣的方面与先前对光谱的基于模型的解释不同。