Literature DB >> 8580351

Intramolecular charge transfer in the bacteriorhodopsin mutants Asp85-->Asn and Asp212-->Asn: effects of pH and anions.

S Moltke1, M P Krebs, R Mollaaghababa, H G Khorana, M P Heyn.   

Abstract

The photovoltage kinetics of the bacteriorhodopsin mutants Asp212-->Asn and Asp85-->Asn after excitation at 580 nm have been investigated in the pH range from 0 to 11. With the mutant Asp85-->Asn (D85N) at pH 7 no net charge translocation is observed and the signal is the same, both in the presence of Cl- (150 mM) and in its absence (75 mM SO4(2-)). Under both conditions the color of the pigment is blue (lambda max = 615 nm). The time course of the photovoltage kinetics is similar to that of the acid-blue form of wild-type, except that an additional transient charge motion occurs with time constants of 60 microseconds and 1.3 ms, indicating the transient deprotonation and reprotonation of an unknown group to and from the extracellular side of the membrane. It is suggested that this is the group XH, which is responsible for proton release in wild-type. At pH 1, the photovoltage signal of D85N changes upon the addition of Cl- from that characteristic for the acid-blue state of wild-type to that characteristic for the acid-purple state. Therefore, the protonation of the group at position at 85 is necessary, but not sufficient for the chloride-binding. At pH 11, well above the pKa of the Schiff base, there is a mixture of "M-like" and "N-like" states. Net proton transport in the same direction as in wild-type is restored in D85N from this N-like state. With the mutant Asp212-->Asn (D212N), time-resolved photovoltage measurements show that in the absence of halide ions the signal is similar to that of the acid-blue form of wild-type and that no net charge translocation occurs in the entire pH range from 0 to 11. Upon addition of Cl- in the pH range from 3.8 to 7.2 the color of the pigment returns to purple and the photovoltage experiments indicate that net proton pumping is restored. However, this Cl(-)-induced activation of net charge-transport in D212N is only partial. Outside this pH range, no net charge transport is observed even in the presence of chloride, and the photovoltage shows the same chloride-dependent features as those accompanying the acid-blue to acid-purple transition of the wild-type.

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Year:  1995        PMID: 8580351      PMCID: PMC1236441          DOI: 10.1016/S0006-3495(95)80078-0

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


  29 in total

1.  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

2.  Pathways of the rise and decay of the M photointermediate(s) of bacteriorhodopsin.

Authors:  G Váró; J K Lanyi
Journal:  Biochemistry       Date:  1990-03-06       Impact factor: 3.162

3.  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

4.  Rapid long-range proton diffusion along the surface of the purple membrane and delayed proton transfer into the bulk.

Authors:  U Alexiev; R Mollaaghababa; P Scherrer; H G Khorana; M P Heyn
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-17       Impact factor: 11.205

5.  Estimated acid dissociation constants of the Schiff base, Asp-85, and Arg-82 during the bacteriorhodopsin photocycle.

Authors:  L S Brown; L Bonet; R Needleman; J K Lanyi
Journal:  Biophys J       Date:  1993-07       Impact factor: 4.033

6.  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

7.  Model for the structure of bacteriorhodopsin based on high-resolution electron cryo-microscopy.

Authors:  R Henderson; J M Baldwin; T A Ceska; F Zemlin; E Beckmann; K H Downing
Journal:  J Mol Biol       Date:  1990-06-20       Impact factor: 5.469

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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  7 in total

1.  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

2.  Spectroscopic study of the transmembrane domain of a rhodopsin-phosphodiesterase fusion protein from a unicellular eukaryote.

Authors:  Masahito Watari; Tatsuya Ikuta; Daichi Yamada; Wataru Shihoya; Kazuho Yoshida; Satoshi P Tsunoda; Osamu Nureki; Hideki Kandori
Journal:  J Biol Chem       Date:  2019-01-08       Impact factor: 5.157

Review 3.  The evolving capabilities of rhodopsin-based genetically encoded voltage indicators.

Authors:  Yiyang Gong
Journal:  Curr Opin Chem Biol       Date:  2015-07-02       Impact factor: 8.822

4.  Coordinating the structural rearrangements associated with unidirectional proton transfer in the bacteriorhodopsin photocycle induced by deprotonation of the proton-release group: a time-resolved difference FTIR spectroscopic study.

Authors:  Joel E Morgan; Ahmet S Vakkasoglu; Janos K Lanyi; Robert B Gennis; Akio Maeda
Journal:  Biochemistry       Date:  2010-04-20       Impact factor: 3.162

5.  Imaging neural spiking in brain tissue using FRET-opsin protein voltage sensors.

Authors:  Yiyang Gong; Mark J Wagner; Jin Zhong Li; Mark J Schnitzer
Journal:  Nat Commun       Date:  2014-04-22       Impact factor: 14.919

6.  A role for internal water molecules in proton affinity changes in the Schiff base and Asp85 for one-way proton transfer in bacteriorhodopsin.

Authors:  Joel E Morgan; Robert B Gennis; Akio Maeda
Journal:  Photochem Photobiol       Date:  2008-06-28       Impact factor: 3.421

7.  Enhanced Archaerhodopsin Fluorescent Protein Voltage Indicators.

Authors:  Yiyang Gong; Jin Zhong Li; Mark J Schnitzer
Journal:  PLoS One       Date:  2013-06-19       Impact factor: 3.240

  7 in total

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