Excitation Energies of a Water-bridged Twisted Retinal Structure in the Bacteriorhodopsin Proton Pump: a Theoretical Investigation
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Chemistry
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The first proton transfer in the bacteriorhodopsin photocycle takes place during the L → M transition. Structural details of the pre proton transfer L intermediate have been investigated using experiments and computations. Here, we assess L-state structural models by performing hybrid quantum mechanical/molecular mechanical molecular dynamics and excitation energy calculations. The computations suggest that a water-bridged twisted retinal structure gives the closest agreement with the experimental L/bR shift in the excitation energy.
Kubar T, Elstner M, Cui Q Annu Rev Biophys. 2023; 52:525-551.
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Active site structure and absorption spectrum of channelrhodopsin-2 wild-type and C128T mutant.
Guo Y, Beyle F, Bold B, Watanabe H, Koslowski A, Thiel W Chem Sci. 2018; 7(6):3879-3891.
PMID: 30155032 PMC: 6013792. DOI: 10.1039/c6sc00468g.
Retinal isomerization and water-pore formation in channelrhodopsin-2.
Ardevol A, Hummer G Proc Natl Acad Sci U S A. 2018; 115(14):3557-3562.
PMID: 29555736 PMC: 5889620. DOI: 10.1073/pnas.1700091115.
Density functional tight binding: values of semi-empirical methods in an ab initio era.
Cui Q, Elstner M Phys Chem Chem Phys. 2014; 16(28):14368-77.
PMID: 24850383 PMC: 4836871. DOI: 10.1039/c4cp00908h.