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中子蛋白质晶体学中的分析仪。

The analyzer in neutron protein crystallography.

作者信息

Nunes A C, Norvell J C

出版信息

Brookhaven Symp Biol. 1976 May(27):VII57-VII66.

PMID:963589
Abstract

The use of a pyrolytic graphite analyzer is shown to contribute to the cleanliness of a neutron protein crystallographic study. If neutrons of approximately 1.5-A wavelength are used, higher orders are reduced by nearly an order of magnitude, and background (arising largely from incoherent inelastic neutron-proton scattering) is reduced by nearly a factor of five. These advantages are gained at the expense of approximately 50% of measured integrated intensity and a distortion of integrated intensity with scattering angle. Because background scatter is generally large compared with peak reflectivity of a protein, the large background reduction by the analyzer more than compensates for reduced peak intensity to improve the statistics of most peak reflectivity measurements. The luminance function distortion of intensity data is not large, produces a slight smearing of atomic scattering density, and can be calculated and adjusted for in the data.

摘要

热解石墨分析仪的使用有助于中子蛋白质晶体学研究的清洁度。如果使用波长约为1.5埃的中子,高阶次会降低近一个数量级,背景(主要源于非相干非弹性中子-质子散射)会降低近五倍。这些优势是以牺牲约50%的测量积分强度以及积分强度随散射角的畸变来实现的。由于与蛋白质的峰值反射率相比,背景散射通常较大,分析仪对背景的大幅降低足以弥补峰值强度的降低,从而改善大多数峰值反射率测量的统计数据。强度数据的亮度函数畸变不大,只会使原子散射密度略有模糊,并且可以在数据中进行计算和调整。

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