Dilanian Ruben A, Streltsov Victor, Coughlan Hannah D, Quiney Harry M, Martin Andrew V, Klonis Nectarios, Dogovski Con, Boutet Sébastien, Messerschmidt Marc, Williams Garth J, Williams Sophie, Phillips Nicholas W, Nugent Keith A, Tilley Leann, Abbey Brian
ARC Centre of Excellence in Advanced Molecular Imaging, School of Physics, The University of Melbourne, Melbourne, Victoria 3010, Australia.
CSIRO, Parkville, Victoria 3052, Australia.
J Appl Crystallogr. 2017 Sep 28;50(Pt 5):1533-1540. doi: 10.1107/S1600576717012663. eCollection 2017 Oct 1.
The recent availability of extremely intense, femtosecond X-ray free-electron laser (XFEL) sources has spurred the development of serial femtosecond nanocrystallography (SFX). Here, SFX is used to analyze nanoscale crystals of β-hematin, the synthetic form of hemozoin which is a waste by-product of the malaria parasite. This analysis reveals significant differences in β-hematin data collected during SFX and synchrotron crystallography experiments. To interpret these differences two possibilities are considered: structural differences between the nanocrystal and larger crystalline forms of β-hematin, and radiation damage. Simulation studies show that structural inhomogeneity appears at present to provide a better fit to the experimental data. If confirmed, these observations will have implications for designing compounds that inhibit hemozoin formation and suggest that, for some systems at least, additional information may be gained by comparing structures obtained from nanocrystals and macroscopic crystals of the same molecule.
近期,超强飞秒X射线自由电子激光(XFEL)源的出现推动了飞秒级串联纳米晶体学(SFX)的发展。在此,SFX被用于分析β-血红素的纳米级晶体,β-血红素是疟原虫的一种废弃副产物——疟色素的合成形式。该分析揭示了在SFX和同步加速器晶体学实验中收集到的β-血红素数据存在显著差异。为了解释这些差异,考虑了两种可能性:β-血红素纳米晶体与较大晶体形式之间的结构差异以及辐射损伤。模拟研究表明,目前结构不均匀性似乎能更好地拟合实验数据。如果得到证实,这些观察结果将对设计抑制疟色素形成的化合物具有启示意义,并表明至少对于某些系统而言,通过比较同一分子的纳米晶体和宏观晶体所获得的结构可能会获得更多信息。