The analyzer in neutron protein crystallography.

Brookhaven symposia in biology Pub Date : 1976-05-01
A C Nunes, J C Norvell
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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.

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中子蛋白结晶学分析仪。
使用热解石墨分析仪有助于中子蛋白晶体学研究的清洁度。如果使用波长约为1.5 a的中子,则高阶降低了近一个数量级,并且背景(主要由非相干非弹性中子-质子散射引起)降低了近五倍。这些优点是以测量的综合强度减少约50%和散射角导致的综合强度失真为代价获得的。由于与蛋白质的峰值反射率相比,背景散射通常较大,因此分析仪的大背景减小量可以补偿降低的峰值强度,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,对原子散射密度产生轻微的涂抹,可以在数据中进行计算和调整。
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