Ultrafast Photoinduced Deactivation Dynamics of Proteorhodopsin

被引:10
|
作者
Eckert, C. Elias [1 ]
Kaur, Jagdeep [2 ]
Glaubitz, Clemens [2 ]
Wachtveitl, Josef [1 ]
机构
[1] Goethe Univ Frankfurt Main, Inst Phys & Theoret Chem, Max von Laue Str 7, D-60438 Frankfurt, Germany
[2] Goethe Univ Frankfurt Main, Inst Biophys Chem, Max von Laue Str 9, D-60438 Frankfurt, Germany
来源
关键词
RESONANCE RAMAN-SPECTROSCOPY; LOW-TEMPERATURE FTIR; RETINAL SCHIFF-BASE; BLUE-LIGHT; BACK PHOTOREACTION; M-INTERMEDIATE; BACTERIORHODOPSIN PHOTOCYCLE; PHOTOCHEMICAL-REACTION; INFRARED-SPECTROSCOPY; PHOTOISOMERIZATION;
D O I
10.1021/acs.jpclett.6b02975
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report femtosecond time-resolved absorption change measurements of the photoinduced deactivation dynamics of a microbial rhodopsin in the ultraviolet visible and mid-infrared range. The blue light quenching process is recorded in green proteorhodopsin's (GPR) primary proton donor mutant E108Q from the deprotonated 13-cis photointermediate. The return of GPR to the dark state occurs in two steps, starting with the photoinduced 13-cis to all-trans reisomerization of the retinal. The subsequent Schiff base reprotonation via the primary proton acceptor (D97) occurs on a nanosecond time scale. This step is two orders of magnitude faster than that in bacteriorhodopsin, potentially because of the very high pK(A) of the GPR primary proton acceptor.
引用
收藏
页码:512 / 517
页数:6
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