Addressing high excitation conditions in time-resolved X-ray diffraction experiments and issues of biological relevance

被引:9
作者
Besaw, Jessica E. [1 ]
Miller, R. J. Dwayne [2 ,3 ]
机构
[1] Univ Toronto, Dept Biochem, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
[3] Univ Toronto, Dept Phys, 80 St George St, Toronto, ON M5S 3H6, Canada
关键词
Time-resolved crystallography; Laser illumination guidelines; Structure-function relationships; MAPPING ATOMIC MOTIONS; BACTERIORHODOPSIN; ELECTRONS; PHOTOISOMERIZATION; CRYSTALLOGRAPHY; ABSORPTION; ENERGY;
D O I
10.1016/j.sbi.2023.102624
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
One of the most important fundamental questions connecting chemistry to biology is how chemistry scales in complexity up to biological systems where there are innumerable possible pathways and competing processes. With the development of ultrabright electron and x-ray sources, it has been possible to literally light up atomic motions to directly observe the reduction in dimensionality in the barrier crossing region to a few key reaction modes. How do these chemical processes further couple to the surrounding protein or macromolecular assembly to drive biological functions? Optical methods to trigger photoactive biological processes are needed to probe this issue on the relevant timescales. However, the excitation conditions have been in the highly nonlinear regime, which questions the biological relevance of the observed structural dynamics.
引用
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页数:12
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