Time-Resolved Macromolecular Crystallography at Pulsed X-ray Sources

被引:41
|
作者
Schmidt, Marius [1 ]
机构
[1] Univ Wisconsin, Phys Dept, Milwaukee, WI 53211 USA
关键词
time-resolved crystallography; serial femtosecond crystallography; Monte Carlo integration; beta-lactamase; bacterial phytochromes; PHOTOACTIVE YELLOW PROTEIN; SERIAL MILLISECOND CRYSTALLOGRAPHY; TRANS-CIS ISOMERIZATION; CRYSTAL-STRUCTURE; LAUE DIFFRACTION; STRUCTURAL-CHANGES; LIGAND-BINDING; PHOTOSYSTEM-II; MYOGLOBIN; DYNAMICS;
D O I
10.3390/ijms20061401
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The focus of structural biology is shifting from the determination of static structures to the investigation of dynamical aspects of macromolecular function. With time-resolved macromolecular crystallography (TRX), intermediates that form and decay during the macromolecular reaction can be investigated, as well as their reaction dynamics. Time-resolved crystallographic methods were initially developed at synchrotrons. However, about a decade ago, extremely brilliant, femtosecond-pulsed X-ray sources, the free electron lasers for hard X-rays, became available to a wider community. TRX is now possible with femtosecond temporal resolution. This review provides an overview of methodological aspects of TRX, and at the same time, aims to outline the frontiers of this method at modern pulsed X-ray sources.
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收藏
页数:23
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