Literature DB >> 23779103

Excitation energies of a water-bridged twisted retinal structure in the bacteriorhodopsin proton pump: a theoretical investigation.

Tino Wolter1, Kai Welke, Prasad Phatak, Ana-Nicoleta Bondar, Marcus Elstner.   

Abstract

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.

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Year:  2013        PMID: 23779103     DOI: 10.1039/c3cp44280b

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  3 in total

1.  Density functional tight binding: values of semi-empirical methods in an ab initio era.

Authors:  Qiang Cui; Marcus Elstner
Journal:  Phys Chem Chem Phys       Date:  2014-07-28       Impact factor: 3.676

2.  Active site structure and absorption spectrum of channelrhodopsin-2 wild-type and C128T mutant.

Authors:  Yanan Guo; Franziska E Beyle; Beatrix M Bold; Hiroshi C Watanabe; Axel Koslowski; Walter Thiel; Peter Hegemann; Marco Marazzi; Marcus Elstner
Journal:  Chem Sci       Date:  2016-02-26       Impact factor: 9.825

3.  Retinal isomerization and water-pore formation in channelrhodopsin-2.

Authors:  Albert Ardevol; Gerhard Hummer
Journal:  Proc Natl Acad Sci U S A       Date:  2018-03-19       Impact factor: 11.205

  3 in total

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