Literature DB >> 3949744

Effects of anion binding on the deprotonation reactions of halorhodopsin.

B Schobert, J K Lanyi, D Oesterhelt.   

Abstract

The retinal Schiff base of halorhodopsin deprotonates with a pKa of 7.4 in 0.5 M Na2SO4 in the dark. In the presence of various anions, such as chloride or nitrate, etc., the pKa is raised by up to 1.5 units. Analysis of the dependency of the pKa on anion concentration favors the model in which the anions do not bind to the positively charged Schiff base nitrogen, but to a site near it, and exert their effect on the pKa by direct (perhaps electrostatic) interaction. Adding nitrate, or one of several other anions, causes also a small blueshift in the visible absorption band of the chromophore. These effects on the pKa and the absorption band define an anion binding site in halorhodopsin, termed Site I. Chloride and bromide apparently bind in addition to another site, which is associated with a small red-shift of the absorption band and changes in the photocycle. This other anion binding site is termed Site II. Illumination of halorhodopsin samples results in the deprotonation of the Schiff base with a much lowered pKa, but at very low rates probably determined by the generation of a deprotonating photointermediate. Binding of Site I anions increases the pKa of deprotonation in the light also. The similarity of the responses of the apparent pKa in the dark and in the light to anion concentration suggests that anion binding to Site I influences deprotonation of the Schiff base similarly in the photointermediate and in the parent halorhodopsin molecule.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3949744

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

Review 1.  Bioenergetics of the Archaea.

Authors:  G Schäfer; M Engelhard; V Müller
Journal:  Microbiol Mol Biol Rev       Date:  1999-09       Impact factor: 11.056

2.  Halorhodopsin pumps Cl- and bacteriorhodopsin pumps protons by a common mechanism that uses conserved electrostatic interactions.

Authors:  Yifan Song; M R Gunner
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-31       Impact factor: 11.205

3.  Anion sensitivity and spectral tuning of cone visual pigments in situ.

Authors:  J Kleinschmidt; F I Harosi
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

Review 4.  A unifying concept for ion translocation by retinal proteins.

Authors:  D Oesterhelt; J Tittor; E Bamberg
Journal:  J Bioenerg Biomembr       Date:  1992-04       Impact factor: 2.945

5.  The photochemical cycle of halorhodopsin: absolute spectra of intermediates obtained by flash photolysis and fast difference spectra measurements.

Authors:  J Tittor; D Oesterhelt; R Maurer; H Desel; R Uhl
Journal:  Biophys J       Date:  1987-12       Impact factor: 4.033

6.  Protonation state of Asp (Glu)-85 regulates the purple-to-blue transition in bacteriorhodopsin mutants Arg-82----Ala and Asp-85----Glu: the blue form is inactive in proton translocation.

Authors:  S Subramaniam; T Marti; H G Khorana
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

7.  Diversity, Mechanism, and Optogenetic Application of Light-Driven Ion Pump Rhodopsins.

Authors:  Keiichi Inoue
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

8.  Chloride binding proteins: mechanistic implications for the oxygen-evolving complex of Photosystem II.

Authors:  W J Coleman
Journal:  Photosynth Res       Date:  1990-01       Impact factor: 3.573

9.  Crystal structure of Halobacterium salinarum halorhodopsin with a partially depopulated primary chloride-binding site.

Authors:  Madeleine Schreiner; Ramona Schlesinger; Joachim Heberle; Hartmut H Niemann
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2016-08-26       Impact factor: 1.056

10.  Effects of various anions on the Raman spectrum of halorhodopsin.

Authors:  C Pande; J K Lanyi; R H Callender
Journal:  Biophys J       Date:  1989-03       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.