Tracking the excited-state time evolution of the visual pigment with multiconfigurational quantum chemistry

被引:234
作者
Frutos, Luis Manuel
Andruniow, Tadeusz
Santoro, Fabrizio
Ferre, Nicolas
Olivucci, Massimo
机构
[1] Univ Siena, Dipartimento Chim, I-53100 Siena, Italy
[2] Bowling Green State Univ, Dept Chem, Bowling Green, OH 43403 USA
[3] Wroclaw Univ Technol, Dept Chem, Inst Phys & Theoret Chem, PL-50370 Wroclaw, Poland
[4] CNR, Ist Proc Chim Fis, I-56124 Pisa, Italy
[5] Univ Aix Marseille 1, CNRS, UMR 6517, Lab Chim Theor & Modelisat Mol, F-13397 Marseille 20, France
关键词
photoisomerization; rhodopsin; vision;
D O I
10.1073/pnas.0701732104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The primary event that initiates vision is the photoinduced isomerization of retinal in the visual pigment rhodopsin (Rh). Here, we use a scaled quantum mechanics/molecular mechanics potential that reproduces the isomerization path determined with multiconfigurational perturbation theory to follow the excited-state evolution of bovine Rh. The analysis of a 140-fs trajectory provides a description of the electronic and geometrical changes that prepare the system for decay to the ground state. The data uncover a complex change of the retinal backbone that, at approximate to 60-fs delay, initiates a space saving "asynchronous bicycle-pedal or crankshaft" motion, leading to a conical intersection on a 110-fs time scale. It is shown that the twisted structure achieved at decay features a momentum that provides a natural route toward the photoRh structure recently resolved by using femtosecond-stimulated Raman spectroscopy.
引用
收藏
页码:7764 / 7769
页数:6
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