Literature DB >> 19431867

Low temperature FTIR study of the Schiff base reprotonation during the M-to-bR backphotoreaction: Asp 85 reprotonates two distinct types of Schiff base species at different temperatures.

H Takei1, Y Gat, M Sheves, A Lewis.   

Abstract

We have applied low temperature difference FTIR spectroscopy to investigate intermediates produced from the M intermediate upon blue light excitation (<480 nm). In agreement with an earlier report by Balashov and Litvin (1981), who studied these intermediates with low temperature visible absorption spectrophotometry, we have observed at least three stages in this backphotoreaction. The initial photoproduct is stable at 100 K, and two products of subsequent thermal reactions are observed upon raising the temperature to 130 and 160 K, respectively.The alterations in the C=N stretching mode of the Schiff base have been identified by isotopically labeling the retinal chromophore, and changes in C=O stretching modes of amino acid residues with acidic side chains have been investigated. Analysis of the C=N stretching mode shows that the Schiff base remains unprotonated after the photochemical reaction at 100 K. Moreover, there are two types of Schiff bases, presumably associated with different bR species, that become thermally reprotonated at 130 and 160 K, respectively. Bands associated with the C=O stretching modes suggest that Asp 85 rather than Asp 96 reprotonates the Schiff base during the M to bR backphotoreaction. This conclusion is consistent with earlier observations that the polarity of electrical signals during this photochemical back reaction is reversed as compared to the thermal regeneration of bR from M.

Entities:  

Year:  1992        PMID: 19431867      PMCID: PMC1262281          DOI: 10.1016/S0006-3495(92)81757-5

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


  29 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.  [New intermediates in the photochemical transformation of rhodopsin].

Authors:  F F Litvin; S P Balashov
Journal:  Biofizika       Date:  1977 Nov-Dec

3.  Bacteriorhodopsin: a molecular photoelectric regulator. Quenching of photovoltaic effect of bimolecular lipid membranes containing bacteriorhodopsin by blue light.

Authors:  B Karvaly; Z Dancsházy
Journal:  FEBS Lett       Date:  1977-04-01       Impact factor: 4.124

4.  The photochemical reaction of the 412 nm chromophore of bacteriorhodopsin.

Authors:  B Hess; D Kuschmitz
Journal:  FEBS Lett       Date:  1977-02-15       Impact factor: 4.124

5.  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

6.  Resonance Raman studies of bovine metarhodopsin I and metarhodopsin II.

Authors:  A G Doukas; B Aton; R H Callender; T G Ebrey
Journal:  Biochemistry       Date:  1978-06-13       Impact factor: 3.162

7.  More evidence that light isomerises the cheomophore of purple membrane protein.

Authors:  J B Hurley; B Becher; T G Ebrey
Journal:  Nature       Date:  1978-03-02       Impact factor: 49.962

8.  Kinetics of the blue light-induced inhibition of photoelectric activity of bacteriorhodopsin.

Authors:  Z Dancsházy; L A Drachev; P Ormos; K Nagy; V P Skulachev
Journal:  FEBS Lett       Date:  1978-12-01       Impact factor: 4.124

9.  Transient photovoltages in purple membrane multilayers. Charge displacement in bacteriorhodopsin and its photointermediates.

Authors:  S B Hwang; J I Korenbrot; W Stoeckenius
Journal:  Biochim Biophys Acta       Date:  1978-05-18

10.  A low temperature investigation of the intermediates of the photocycle of light-adapted bacteriorhodopsin. Optical absorption and fluorescence measurements.

Authors:  A N Kriebel; T Gillbro; U P Wild
Journal:  Biochim Biophys Acta       Date:  1979-04-11
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  5 in total

1.  The M intermediate of Pharaonis phoborhodopsin is photoactive.

Authors:  S P Balashov; M Sumi; N Kamo
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

2.  Different modes of proton translocation by sensory rhodopsin I.

Authors:  U Haupts; E Bamberg; D Oesterhelt
Journal:  EMBO J       Date:  1996-04-15       Impact factor: 11.598

3.  Evidence for the first phase of the reprotonation switch of bacteriorhodopsin from time-resolved photovoltage and flash photolysis experiments on the photoreversal of the M-intermediate.

Authors:  S Dickopf; M P Heyn
Journal:  Biophys J       Date:  1997-12       Impact factor: 4.033

4.  Fourier transform infrared double-flash experiments resolve bacteriorhodopsin's M1 to M2 transition.

Authors:  B Hessling; J Herbst; R Rammelsberg; K Gerwert
Journal:  Biophys J       Date:  1997-10       Impact factor: 4.033

5.  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

  5 in total

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