Literature DB >> 8580350

Photovoltage kinetics of the acid-blue and acid-purple forms of bacteriorhodopsin: evidence for no net charge transfer.

S Moltke1, M P Heyn.   

Abstract

Time-resolved photovoltage measurements were performed with the acid-blue (bR605A) and acid-purple (bR565A) forms of bacteriorhodopsin (bR) in the time range from 25 ns to 100 s. The bR605A and bR565A pigments were formed by titration with H2SO4 in the absence and presence of 150 mM KCI, respectively. Qualitatively the kinetics of the charge displacement in these two states are similar and consist of two fast phases in one direction (100 ns bandwidth limited and approximately 1 microsecond) followed by a decay in the opposite direction via one component for bR605A (4.4 +/- 0.6 ms) or two components for bR565A (33 +/- 8 microseconds and 3.6 +/- 0.5 ms). The transient photovoltage signal returns exactly to the initial value after several milliseconds, well before the passive discharge of the electrical measuring system at 2 s. We conclude that no net charge transfer occurs in either bR605A or bR565A. The direction of the fast components is opposite that of net proton translocation in bR at pH 7. So, if the charge that moves back and forth is due to a proton, it moves first in the direction of the cytoplasmic side of the membrane (< 1 microsecond) and returns to its initial position via the 4.4 ms (bR605A) or the 33 microseconds and 3.6 ms (bR565A) decay components. The amplitude of the charge motion in both low pH forms is too large to be due to isomerization alone and is comparable to one of the major components in bR at pH 7.2

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Year:  1995        PMID: 8580350      PMCID: PMC1236440          DOI: 10.1016/S0006-3495(95)80077-9

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  24 in total

1.  Alternative translocation of protons and halide ions by bacteriorhodopsin.

Authors:  A Dér; S Száraz; R Tóth-Boconádi; Z Tokaji; L Keszthelyi; W Stoeckenius
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-01       Impact factor: 11.205

2.  Substitution of amino acids Asp-85, Asp-212, and Arg-82 in bacteriorhodopsin affects the proton release phase of the pump and the pK of the Schiff base.

Authors:  H Otto; T Marti; M Holz; T Mogi; L J Stern; F Engel; H G Khorana; M P Heyn
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

3.  The purple to blue transition of bacteriorhodopsin is accompanied by a loss of the hexagonal lattice and a conformational change.

Authors:  M P Heyn; C Dudda; H Otto; F Seiff; I Wallat
Journal:  Biochemistry       Date:  1989-11-14       Impact factor: 3.162

4.  Photocurrent measurements of the purple membrane oriented in a polyacrylamide gel.

Authors:  S Y Liu; T G Ebrey
Journal:  Biophys J       Date:  1988-08       Impact factor: 4.033

5.  Proton transfer from Asp-96 to the bacteriorhodopsin Schiff base is caused by a decrease of the pKa of Asp-96 which follows a protein backbone conformational change.

Authors:  Y Cao; G Váró; A L Klinger; D M Czajkowsky; M S Braiman; R Needleman; J K Lanyi
Journal:  Biochemistry       Date:  1993-03-02       Impact factor: 3.162

6.  Effect of acid pH on the absorption spectra and photoreactions of bacteriorhodopsin.

Authors:  P C Mowery; R H Lozier; Q Chae; Y W Tseng; M Taylor; W Stoeckenius
Journal:  Biochemistry       Date:  1979-09-18       Impact factor: 3.162

7.  Solid-state 13C and 15N NMR study of the low pH forms of bacteriorhodopsin.

Authors:  H J de Groot; S O Smith; J Courtin; E van den Berg; C Winkel; J Lugtenburg; R G Griffin; J Herzfeld
Journal:  Biochemistry       Date:  1990-07-24       Impact factor: 3.162

8.  Aspartic acid substitutions affect proton translocation by bacteriorhodopsin.

Authors:  T Mogi; L J Stern; T Marti; B H Chao; H G Khorana
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

9.  The retinylidene Schiff base counterion in bacteriorhodopsin.

Authors:  T Marti; S J Rösselet; H Otto; M P Heyn; H G Khorana
Journal:  J Biol Chem       Date:  1991-10-05       Impact factor: 5.157

10.  Anion binding to the Schiff base of the bacteriorhodopsin mutants Asp-85----Asn/Asp-212----Asn and Arg-82----Gln/Asp-85----Asn/Asp-212----Asn.

Authors:  T Marti; H Otto; S J Rösselet; M P Heyn; H G Khorana
Journal:  J Biol Chem       Date:  1992-08-25       Impact factor: 5.157

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  8 in total

1.  Electrical-to-mechanical coupling in purple membranes: membrane as electrostrictive medium.

Authors:  P Kietis; M Vengris; L Valkunas
Journal:  Biophys J       Date:  2001-04       Impact factor: 4.033

2.  Control of the pump cycle in bacteriorhodopsin: mechanisms elucidated by solid-state NMR of the D85N mutant.

Authors:  Mary E Hatcher; Jingui G Hu; Marina Belenky; Peter Verdegem; Johan Lugtenburg; Robert G Griffin; Judith Herzfeld
Journal:  Biophys J       Date:  2002-02       Impact factor: 4.033

3.  Binding of calcium ions to bacteriorhodopsin.

Authors:  G Váró; L S Brown; R Needleman; J K Lanyi
Journal:  Biophys J       Date:  1999-06       Impact factor: 4.033

4.  Green proteorhodopsin reconstituted into nanoscale phospholipid bilayers (nanodiscs) as photoactive monomers.

Authors:  Matthew J Ranaghan; Christine T Schwall; Nathan N Alder; Robert R Birge
Journal:  J Am Chem Soc       Date:  2011-10-26       Impact factor: 15.419

5.  Chloride ion binding to bacteriorhodopsin at low pH: an infrared spectroscopic study.

Authors:  L Kelemen; P Galajda; S Száraz; P Ormos
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

6.  Specific binding sites for cations in bacteriorhodopsin.

Authors:  T Eliash; L Weiner; M Ottolenghi; M Sheves
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

7.  Photocycle of dried acid purple form of bacteriorhodopsin.

Authors:  G I Groma; L Kelemen; A Kulcsár; M Lakatos; G Váró
Journal:  Biophys J       Date:  2001-12       Impact factor: 4.033

8.  Bacteriorhodopsin-ZnO hybrid as a potential sensing element for low-temperature detection of ethanol vapour.

Authors:  Saurav Kumar; Sudeshna Bagchi; Senthil Prasad; Anupma Sharma; Ritesh Kumar; Rishemjit Kaur; Jagvir Singh; Amol P Bhondekar
Journal:  Beilstein J Nanotechnol       Date:  2016-04-04       Impact factor: 3.649

  8 in total

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