The minimum crystal size needed for a complete diffraction data set

被引:146
作者
Holton, James M. [1 ,2 ]
Frankel, Kenneth A. [2 ]
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[2] Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2010年 / 66卷
基金
美国国家卫生研究院;
关键词
X-RAY-ABSORPTION; RADIATION-DAMAGE; PROTEIN CRYSTALS; DATA-COLLECTION; MACROMOLECULAR CRYSTALLOGRAPHY; SYNCHROTRON-RADIATION; DOSE CALCULATIONS; AREA DETECTOR; REFLECTION; REFINEMENT;
D O I
10.1107/S0907444910007262
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, classic intensity formulae were united with an empirical spot-fading model in order to calculate the diameter of a spherical crystal that will scatter the required number of photons per spot at a desired resolution over the radiation-damage-limited lifetime. The influences of molecular weight, solvent content, Wilson B factor, X-ray wavelength and attenuation on scattering power and dose were all included. Taking the net photon count in a spot as the only source of noise, a complete data set with a signal-to-noise ratio of 2 at 2 A resolution was predicted to be attainable from a perfect lysozyme crystal sphere 1.2 mm in diameter and two different models of photoelectron escape reduced this to 0.5 or 0.34 mm. These represent 15-fold to 700-fold less scattering power than the smallest experimentally determined crystal size to date, but the gap was shown to be consistent with the background scattering level of the relevant experiment. These results suggest that reduction of background photons and diffraction spot size on the detector are the principal paths to improving crystallographic data quality beyond current limits.
引用
收藏
页码:393 / 408
页数:16
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