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Settling the Long-Standing Debate on the Proton Storage Site of the Prototype Light-Driven Proton Pump Bacteriorhodopsin
- Source :
- The Journal of Physical Chemistry B. 123:9598-9608
- Publication Year :
- 2019
- Publisher :
- American Chemical Society (ACS), 2019.
-
Abstract
- Despite decades of research, the location and molecular identity of the proton release group together with the subsequent proton release pathway remain controversial even for the simplest light-driven proton pump, bacteriorhodopsin, according to the most recent experiments and simulations. Yet despite this nagging lack of knowledge for the generic case, even more complex pumps are currently under investigation. The proton release group disclosed by our large-scale simulations satisfies available experimental results, especially the broad Zundel continuum absorption subject to a striking anisotropy observed only recently. Moreover, our simulations delineate the seamless pathway by which the excess proton (being stored in an ultrastrong centered H-bond involving two glutamates) is finally translocated into the extracellular medium.
- Subjects :
- Halobacterium salinarum
Continuum absorption
Proton
Molecular Dynamics Simulation
010402 general chemistry
01 natural sciences
Glutamates
0103 physical sciences
Materials Chemistry
Lack of knowledge
Physical and Theoretical Chemistry
Density Functional Theory
Physics
Binding Sites
Ion Transport
010304 chemical physics
biology
Bacteriorhodopsin
0104 chemical sciences
Surfaces, Coatings and Films
Models, Chemical
Chemical physics
Bacteriorhodopsins
biology.protein
Light driven
Protons
Protein Binding
Subjects
Details
- ISSN :
- 15205207 and 15206106
- Volume :
- 123
- Database :
- OpenAIRE
- Journal :
- The Journal of Physical Chemistry B
- Accession number :
- edsair.doi.dedup.....0ef453b548295ca90e4a414bb3c7fd8c
- Full Text :
- https://doi.org/10.1021/acs.jpcb.9b09608