Literature DB >> 7758451

The ability of actinic light to modify the bacteriorhodopsin photocycle. Heterogeneity and/or photocooperativity?

R I Shrager1, R W Hendler, S Bose.   

Abstract

The focus of this paper is on the established observation that the bacteriorhodopsin (BR) photocycle responds to the level of actinic light by altering the proportions of two forms of the M intermediate. The first form of M, called M-fast or MF, decays to the O intermediate. In contrast, the second form of M, called M-slow or MS, decays directly to the ground state, and its decay rate is slower than that of MF. Any proposed scheme for the BR photocycle must account for this light-dependent phenomenon. Several papers have attempted to explain the observation on the basis of photocooperativity, or on the basis of heterogeneous populations. In this paper, we test previously proposed cooperative models with experimental data, and find those models to be inadequate. We show that two new models, one purely cooperative, the other purely heterogeneous, can both fit the data, hence such modelling will not resolve the mechanism. Taking into account the demonstration of heterogeneity, the trimer structure of BR, and certain experimental evidence in favor of cooperativity, it appears likely that both heterogeneity and cooperativity are involved in the adaptation of the BR photocycle to different levels of actinic light.

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Year:  1995        PMID: 7758451     DOI: 10.1111/j.1432-1033.1995.tb20502.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  6 in total

1.  Structure of the bacteriorhodopsin mutant F219L N intermediate revealed by electron crystallography.

Authors:  J Vonck
Journal:  EMBO J       Date:  2000-05-15       Impact factor: 11.598

2.  Simultaneous measurements of fast optical and proton current kinetics in the bacteriorhodopsin photocycle using an enhanced spectrophotometer.

Authors:  John W Kakareka; Paul D Smith; Thomas J Pohida; Richard W Hendler
Journal:  J Biochem Biophys Methods       Date:  2007-11-17

3.  The ability of actinic light to modify the bacteriorhodopsin photocycle revisited: heterogeneity vs photocooperativity.

Authors:  Richard W Hendler; Richard I Shrager; Curtis W Meuse
Journal:  Biochemistry       Date:  2008-04-19       Impact factor: 3.162

4.  Electrogenic proton-pumping capabilities of the m-fast and m-slow photocycles of bacteriorhodopsin.

Authors:  Richard W Hendler; Curtis W Meuse
Journal:  Biochemistry       Date:  2008-04-19       Impact factor: 3.162

5.  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

6.  Lipid patches in membrane protein oligomers: crystal structure of the bacteriorhodopsin-lipid complex.

Authors:  L Essen; R Siegert; W D Lehmann; D Oesterhelt
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-29       Impact factor: 11.205

  6 in total

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