Photocycle of Cyanobacteriochrome TePixJ

被引:6
|
作者
Hardman, Samantha J. O. [1 ,2 ]
Heyes, Derren J. [1 ,2 ]
Sazanovich, Igor, V [3 ]
Scrutton, Nigel S. [1 ,2 ]
机构
[1] Univ Manchester, Fac Sci & Engn, Manchester Inst Biotechnol, Sch Nat Sci, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Fac Sci & Engn, Dept Chem, Sch Nat Sci, Manchester M1 7DN, Lancs, England
[3] Sci & Technol Facil Council, Res Complex Harwell, Cent Laser Facil, Didcot OX11 0QX, Oxon, England
基金
英国科学技术设施理事会; 英国生物技术与生命科学研究理事会;
关键词
FEMTOSECOND PHOTODYNAMICS; EXCITED-STATE; PHOTOCONVERSION; PHYTOCHROME; CHROMOPHORE; BLUE; CRYSTALLOGRAPHY; NPR6012G4; MECHANISM; DYNAMICS;
D O I
10.1021/acs.biochem.0c00382
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
Due to the recent advances in X-ray free electron laser techniques, bilin-containing cyanobacteriochrome photoreceptors have become prime targets for the ever-expanding field of time-resolved structural biology. However, to facilitate these challenging studies, it is essential that the time scales of any structural changes during the photocycles of cyanobacteriochromes be established. Here, we have used visible and infrared transient absorption spectroscopy to probe the photocycle of a model cyanobacteriochrome system, TePixJ. The kinetics span multiple orders of magnitude from picoseconds to seconds. Localized changes in the bilin binding pocket occur in picoseconds to nanoseconds, followed by more large-scale changes in protein structure, including formation and breakage of a second thioether linkage, in microseconds to milliseconds. The characterization of the entire photocycle will provide a vital frame of reference for future time-resolved structural studies of this model photoreceptor.
引用
收藏
页码:2909 / 2915
页数:7
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