Literature DB >> 2819234

Photocycles of bacteriorhodopsin in light- and dark-adapted purple membrane studied by time-resolved absorption spectroscopy.

J Hofrichter1, E R Henry, R H Lozier.   

Abstract

Nanosecond time-resolved absorption spectra have been measured throughout the photocycle of bacteriorhodopsin in both light-adapted and dark-adapted purple membrane (PM). The data from dark-adapted samples are interpretable as the superposition of two photocycles arising independently from the all-trans and 13-cis retinal isomers that coexist in the dark-adapted state. The presence of a photocycle in dark-adapted PM which is indistinguishable from that observed for light-adapted PM under the same experimental conditions is demonstrated by the observation of the same five relaxation rates associated with essentially identical changes in the photoproduct spectra. This cycle is attributed to the all-trans component. The cycle of the 13-cis component is revealed by scaling the data measured for the light-adapted sample and subtracting it from the data on the dark-adapted mixture. At times less than 1 ms, the resulting difference spectra are nearly time-independent. The peak of the difference spectrum is near 600 nm, although there appears to be a slight (approximately 2 nm) blue-shift in the first few microseconds. Subsequently the amplitude of this spectrum decays and the peak of the difference spectrum shifts in two relaxations. Most of the amplitude of the photoproduct difference spectrum (approximately 80%) decays in a single relaxation having a time constant of approximately 35 ms. The difference spectrum remaining after this relaxation peaks at approximately 590 nm and is indistinguishable from the classical light-dark difference spectrum, which we find, in experiments performed on a much longer time scale, to peak at 588 nm. The decay of this remaining photo-product is not resolvable in the nanosecond kinetic experiments, but dark adaptation of a completely light-adapted sample is found to occur exponentially with a relaxation time of approximately 2,000 s under the conditions of our experiments.

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Year:  1989        PMID: 2819234      PMCID: PMC1280525          DOI: 10.1016/S0006-3495(89)82716-X

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


  22 in total

1.  Bacteriorhodopsin: a light-driven proton pump in Halobacterium Halobium.

Authors:  R H Lozier; R A Bogomolni; W Stoeckenius
Journal:  Biophys J       Date:  1975-09       Impact factor: 4.033

2.  Photochemistry and dark equilibrium of retinal isomers and bacteriorhodopsin isomers.

Authors:  W Sperling; P Carl; Ch Rafferty; N A Dencher
Journal:  Biophys Struct Mech       Date:  1977-06-29

3.  The effect of quaternary structure on the kinetics of conformational changes and nanosecond geminate rebinding of carbon monoxide to hemoglobin.

Authors:  L P Murray; J Hofrichter; E R Henry; M Ikeda-Saito; K Kitagishi; T Yonetani; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

Review 4.  Bacteriorhodopsin and the purple membrane of halobacteria.

Authors:  W Stoeckenius; R H Lozier; R A Bogomolni
Journal:  Biochim Biophys Acta       Date:  1979-03-14

5.  Tyrosine protonation changes in bacteriorhodopsin. A Fourier transform infrared study of BR548 and its primary photoproduct.

Authors:  P D Roepe; P L Ahl; J Herzfeld; J Lugtenburg; K J Rothschild
Journal:  J Biol Chem       Date:  1988-04-15       Impact factor: 5.157

6.  Resonance Raman spectra of bacteriorhodopsin's primary photoproduct: evidence for a distorted 13-cis retinal chromophore.

Authors:  M Braiman; R Mathies
Journal:  Proc Natl Acad Sci U S A       Date:  1982-01       Impact factor: 11.205

7.  Procedure for testing kinetic models of the photocycle of bacteriorhodopsin.

Authors:  J F Nagle; L A Parodi; R H Lozier
Journal:  Biophys J       Date:  1982-05       Impact factor: 4.033

8.  Are C14-C15 single bond isomerizations of the retinal chromophore involved in the proton-pumping mechanism of bacteriorhodopsin?

Authors:  S O Smith; I Hornung; R van der Steen; J A Pardoen; M S Braiman; J Lugtenburg; R A Mathies
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

9.  Action spectrum and quantum efficiency for proton pumping in Halobacterium halobium.

Authors:  R A Bogomolni; R A Baker; R H Lozier; W Stoeckenius
Journal:  Biochemistry       Date:  1980-05-13       Impact factor: 3.162

10.  Nanosecond optical spectra of iron-cobalt hybrid hemoglobins: geminate recombination, conformational changes, and intersubunit communication.

Authors:  J Hofrichter; E R Henry; J H Sommer; R Deutsch; M Ikeda-Saito; T Yonetani; W A Eaton
Journal:  Biochemistry       Date:  1985-05-21       Impact factor: 3.162

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  21 in total

Review 1.  Proton transfer and energy coupling in the bacteriorhodopsin photocycle.

Authors:  J K Lanyi
Journal:  J Bioenerg Biomembr       Date:  1992-04       Impact factor: 2.945

2.  Uv-visible spectroscopy of bacteriorhodopsin mutants: substitution of Arg-82, Asp-85, Tyr-185, and Asp-212 results in abnormal light-dark adaptation.

Authors:  M Duñach; T Marti; H G Khorana; K J Rothschild
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

3.  Solving complex photocycle kinetics. Theory and direct method.

Authors:  J F Nagle
Journal:  Biophys J       Date:  1991-02       Impact factor: 4.033

4.  A microbial rhodopsin with a unique retinal composition shows both sensory rhodopsin II and bacteriorhodopsin-like properties.

Authors:  Yuki Sudo; Kunio Ihara; Shiori Kobayashi; Daisuke Suzuki; Hiroki Irieda; Takashi Kikukawa; Hideki Kandori; Michio Homma
Journal:  J Biol Chem       Date:  2010-12-06       Impact factor: 5.157

5.  Assay of bacteriorhodopsin stability on polycarbonate surface by using of FTIR-ATR: a model of disk-based bioassays.

Authors:  Ahmad Molaeirad; Amineh Leilabadi Asl; Maryam Khayati; Mahdi Alijanianzadeh
Journal:  J Bioenerg Biomembr       Date:  2015-07-08       Impact factor: 2.945

6.  Reversible steps in the bacteriorhodopsin photocycle.

Authors:  R H Lozier; A Xie; J Hofrichter; G M Clore
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-15       Impact factor: 11.205

7.  Two-photon absorption of bacteriorhodopsin: formation of a red-shifted thermally stable photoproduct F620.

Authors:  Thorsten Fischer; Norbert A Hampp
Journal:  Biophys J       Date:  2005-05-13       Impact factor: 4.033

8.  Correlation between absorption maxima and thermal isomerization rates in bacteriorhodopsin.

Authors:  S J Milder
Journal:  Biophys J       Date:  1991-08       Impact factor: 4.033

9.  Pressure effects on the dark-adaptation of bacteriorhodopsin.

Authors:  I Kovács; G U Nienhaus; R Philipp; A Xie
Journal:  Biophys J       Date:  1993-04       Impact factor: 4.033

10.  Quantum efficiency of the photochemical cycle of bacteriorhodopsin.

Authors:  R Govindjee; S P Balashov; T G Ebrey
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

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