Phasing in the presence of severe-site specific radiation damage through dose-dependent modelling of heavy atoms

被引:49
作者
Schiltz, M
Dumas, P
Ennifar, E
Flensburg, C
Paciorek, W
Vonrhein, C
Bricogne, G
机构
[1] Ecole Polytech Fed Lausanne, Lab Cristallog, FSB,IPMC, LCR, CH-1015 Lausanne, Switzerland
[2] Global Phasing Ltd, Cambridge CB3 0AX, England
[3] CNRS, UPR 9002, Inst Biol Mol & Cellulaire, F-67084 Strasbourg, France
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2004年 / 60卷
关键词
D O I
10.1107/S0907444904006377
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The case of a brominated RNA crystal structure determination in which standard three-wavelength MAD phasing was unsuccessful because of fast X-ray-induced debromination was reinvestigated [Ennifar et al. ( 2002), Acta Cryst. D58, 1262 - 1268]. It was found that if the data are kept unmerged and if a dose-stamp is associated with each reflection measurement, dose-dependent occupancies can be refined for the Br atoms. Such a parametrization has been implemented in the macromolecular phasing program SHARP. Re ning such dose-dependent occupancies on an unmerged data set gave a dramatic improvement, even for SAD phases from only the first wavelength (peak), and resulted in a good electron-density map after solvent flattening. The adverse effect of radiation damage has been turned into a beneficial one. The crucial difference is made by the use of unmerged data: phasing power is generated through the intensity differences of symmetry-related reflections recorded at different doses, i.e. corresponding to different states of the X-ray-induced debromination. This approach should prove useful in all situations of experimental phasing where site-specific radiation damage occurs unavoidably and undesirably and not only in cases in which radiation damage is purposely being created in order to demonstrate its potential usefulness.
引用
收藏
页码:1024 / 1031
页数:8
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