Literature DB >> 698342

Primary intermediates in the photochemical cycle of bacteriorhodopsin.

M L Applebury, K S Peters, P M Rentzepis.   

Abstract

Picosecond studies of the primary photochemical events in the light-adapted bacteriorhodopsin, bR570, indicate that the first metastable intermediate K610 is formed with a rise time of 11 ps. Difference spectra obtained at 50 ps after excitation show that K610 is the same species as that trapped in low temperature glasses. A precursor species (S) of the K610 intermediate has been observed which is red shifted with respect to K610 and is formed within the 6-ps time width of the excitation pulse. The formation of the precursor has no observable thermal dependence between 298 degrees and 1.8 degrees K. The formation of K610 has a very low thermal barrier and at very low temperatures, the rate of formation becomes practically temperature independent which is characteristic of a tunneling process. The rate of formation becomes practically temperature independent which is characteristic of a tunneling process. The rate of formation of K610 has a moderate deuterium isotope effect of kH/kD approximately 1.6 at 298 degrees K and 2.4 at 4 degrees K. The mechanism for formation of K610 is found to involve a rate-limiting proton transfer which occurs by tunneling at low temperatures.

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Year:  1978        PMID: 698342      PMCID: PMC1473525          DOI: 10.1016/S0006-3495(78)85456-3

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


  18 in total

1.  Pre-lumirhodopsin and the bleaching of visual pigments.

Authors:  T YOSHIZAWA; G WALD
Journal:  Nature       Date:  1963-03-30       Impact factor: 49.962

2.  Primary photochemical event in vision: proton translocation.

Authors:  K Peters; M L Applebury; P M Rentzepis
Journal:  Proc Natl Acad Sci U S A       Date:  1977-08       Impact factor: 11.205

3.  Why study nutrition history?

Authors:  G M Briggs
Journal:  Fed Proc       Date:  1977-05

Review 4.  The purple membrane from Halobacterium halobium.

Authors:  R Henderson
Journal:  Annu Rev Biophys Bioeng       Date:  1977

5.  Kinetics of rhodopsin at room temperature measured by picosecond spectroscopy.

Authors:  V Sundstrom; P M Rentzepis; K Peters; M L Applebury
Journal:  Nature       Date:  1977-06-16       Impact factor: 49.962

6.  The quantum efficiency for the photochemical conversion of the purple membrane protein.

Authors:  B Becher; T G Ebrey
Journal:  Biophys J       Date:  1977-02       Impact factor: 4.033

7.  The quantum efficiency of the bacteriorhodopsin photocycle.

Authors:  C R Goldschmidt; O Kalisky; T Rosenfeld; M Ottolenghi
Journal:  Biophys J       Date:  1977-02       Impact factor: 4.033

8.  Kinetics of the 580-nm ultrafast bacteriorhodopsin transient.

Authors:  K J Kaufmann; V Sundstrom; T Yamane; P M Rentzepis
Journal:  Biophys J       Date:  1978-04       Impact factor: 4.033

9.  Temperature and wavelength effects on the photochemistry of rhodopsin, isorhodopsin, bacteriorhodopsin and their photoproducts.

Authors:  J B Hurley; T G Ebrey; B Honig; M Ottolenghi
Journal:  Nature       Date:  1977-12-08       Impact factor: 49.962

10.  Kinetic isotope effects in the photochemical cycle of bacteriorhodopsin.

Authors:  R Korenstein; W V Sherman; S R Caplan
Journal:  Biophys Struct Mech       Date:  1976-12-22
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  22 in total

1.  Time-resolved resonance Raman spectroscopy of intermediates of bacteriorhodopsin: The bK(590) intermediate.

Authors:  J Terner; C L Hsieh; A R Burns; M A El-Sayed
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

2.  Subpicosecond resonance Raman spectra of the early intermediates in the photocycle of bacteriorhodopsin.

Authors:  R van den Berg; H C Bitting; M A El-Sayed
Journal:  Biophys J       Date:  1990-07       Impact factor: 4.033

3.  Early picosecond events in the photocycle of bacteriorhodopsin.

Authors:  H J Polland; M A Franz; W Zinth; W Kaiser; E Kölling; D Oesterhelt
Journal:  Biophys J       Date:  1986-03       Impact factor: 4.033

4.  Nanosecond photolytic interruption of bacteriorhodopsin photocycle: K-590 --> BR-570 reaction.

Authors:  V Bazhenov; P Schmidt; G H Atkinson
Journal:  Biophys J       Date:  1992-06       Impact factor: 4.033

5.  Quantum efficiencies of bacteriorhodopsin photochemical reactions.

Authors:  A H Xie
Journal:  Biophys J       Date:  1990-11       Impact factor: 4.033

6.  Cytochrome oxidation in bacterial photosynthesis.

Authors:  M Bixon; J Jortner
Journal:  Photosynth Res       Date:  1989-01       Impact factor: 3.573

7.  Picosecond time-resolved fluorescence spectroscopy of K-590 in the bacteriorhodopsin photocycle.

Authors:  G H Atkinson; D Blanchard; H Lemaire; T L Brack; H Hayashi
Journal:  Biophys J       Date:  1989-02       Impact factor: 4.033

Review 8.  Synthetic retinals as probes for the binding site and photoreactions in rhodopsins.

Authors:  M Ottolenghi; M Sheves
Journal:  J Membr Biol       Date:  1989-12       Impact factor: 1.843

9.  Photochemistry of rhodopsin and isorhodopsin investigated on a picosecond time scale.

Authors:  T G Monger; R R Alfano; R H Callender
Journal:  Biophys J       Date:  1979-07       Impact factor: 4.033

10.  Excited-state dynamics of bacteriorhodopsin.

Authors:  T Kouyama; K Kinosita; A Ikegami
Journal:  Biophys J       Date:  1985-01       Impact factor: 4.033

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