Literature DB >> 8347577

Pathway of proton uptake in the bacteriorhodopsin photocycle.

L Zimányi1, Y Cao, R Needleman, M Ottolenghi, J K Lanyi.   

Abstract

The time courses of chromophore reactions and proton uptake in the second half of the photocycle of the proton pump bacteriorhodopsin (BR) were examined. At pH > 8.5, the kinetics are simplified by the fact that only the M and N intermediates accumulate. The relaxation kinetics after perturbation of M with a second, blue flash confirm that M<==>N equilibration is the only significant cause of the biphasic M decay. With this feature, the analysis of time-resolved difference spectra yields a scheme which contains two sequential N states connected by a nearly unidirectional reaction. The proton uptake from the bulk, as measured with the pH-indicator dye pyranine, occurs during the decay of the first N rather than the recovery of BR. The results thus suggest the model M2(-1)<==>N(-1) + H+ (from the bulk)<==>N(0)-->BR, where the superscripts indicate the protonation state of the protein relative to BR. M2(-1)-->N(-1) is reprotonation of the Schiff base from D96, N(-1) + H+ (from the bulk)-->N(0) is uptake of proton from the cytoplasmic side, and N(0)-->BR represents 13-cis to all-trans reisomerization of the retinal and other relaxations which regenerate the initial state. R227, a residue near D96, affects the deprotonation of D96 more than the subsequent proton uptake. According to the changed [M2(-1)]/[N(-1)] equilibrium in the R227Q protein, interaction between R227 and D96 is responsible for about 1 pH unit of the decrease in the pKa of D96 during the reprotonation of the Schiff base. According to the pH dependencies of the rate constants in the N(-1)<==>N(0) equilibrium in wild-type and R227Q, interaction with R227 lowers the pKa for proton uptake from the bulk by 0.5 pH unit, to 11. We conclude from the proton uptake kinetics that at physiological pH free energy is converted to proton electrochemical potential in this pump not only as protons are released on the extracellular side [Zimányi, L., Váró. G., Chang, M., Ni, B., Needleman, R., & Lanyi, J. K. (1992) Biochemistry 31, 8535-8543] but also as protons are taken up on the cytoplasmic side.

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Year:  1993        PMID: 8347577     DOI: 10.1021/bi00081a010

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  16 in total

1.  Bacteriorhodopsin photocycle at cryogenic temperatures reveals distributed barriers of conformational substates.

Authors:  Andrei K Dioumaev; Janos K Lanyi
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-29       Impact factor: 11.205

2.  The EF loop in green proteorhodopsin affects conformation and photocycle dynamics.

Authors:  Michaela Mehler; Frank Scholz; Sandra J Ullrich; Jiafei Mao; Markus Braun; Lynda J Brown; Richard C D Brown; Sarah A Fiedler; Johanna Becker-Baldus; Josef Wachtveitl; Clemens Glaubitz
Journal:  Biophys J       Date:  2013-07-16       Impact factor: 4.033

3.  Structure of the N intermediate of bacteriorhodopsin revealed by x-ray diffraction.

Authors:  H Kamikubo; M Kataoka; G Váró; T Oka; F Tokunaga; R Needleman; J K Lanyi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

4.  Determination of the transiently lowered pKa of the retinal Schiff base during the photocycle of bacteriorhodopsin.

Authors:  L S Brown; J K Lanyi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

5.  Kinetic and thermodynamic study of the bacteriorhodopsin photocycle over a wide pH range.

Authors:  K Ludmann; C Gergely; G Váró
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

6.  Electric signals during the bacteriorhodopsin photocycle, determined over a wide pH range.

Authors:  K Ludmann; C Gergely; A Dér; G Váró
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

7.  Protein structural change at the cytoplasmic surface as the cause of cooperativity in the bacteriorhodopsin photocycle.

Authors:  G Váró; R Needleman; J K Lanyi
Journal:  Biophys J       Date:  1996-01       Impact factor: 4.033

8.  The role of water in the extracellular half channel of bacteriorhodopsin.

Authors:  C Ganea; C Gergely; K Ludmann; G Váró
Journal:  Biophys J       Date:  1997-11       Impact factor: 4.033

9.  Connectivity of the retinal Schiff base to Asp85 and Asp96 during the bacteriorhodopsin photocycle: the local-access model.

Authors:  L S Brown; A K Dioumaev; R Needleman; J K Lanyi
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

10.  Switch from conventional to distributed kinetics in the bacteriorhodopsin photocycle.

Authors:  Andrei K Dioumaev; Janos K Lanyi
Journal:  Biochemistry       Date:  2008-09-27       Impact factor: 3.162

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