Literature DB >> 13346044

Acid-base properties of rhodopsin and opsin.

C M RADDING, G WALD.   

Abstract

Purified preparations of cattle rhodopsin have been titrated to various pH, irradiated, and the pH changes followed thereafter until completed. In this way we have obtained the titration curves of rhodopsin, of the immediate product of irradiation, measured within 30 seconds; and of the final product of irradiation (opsin). The rhodopsin preparations display about 54 titratable groups per mole of pigment: about 34 base-binding and 20 acid-binding groups. In default of an absolute purification, one cannot be sure that all of these go with rhodopsin itself. Exposure to light induces an immediate rise of pH between pH 2 and 8, maximal at about pH 5. This-followed by its slow partial or complete reversal-is the only change of pH in the physiological range (6-7). It involves the exposure of 1 new acid-binding group per mole of rhodopsin with pK about 6.6, close therefore to that of the imidazole group of histidine. At acid and alkaline pH this immediate change is followed by slower changes, occupying up to 40 minutes at 20 degrees C. These changes are always in the direction of neutrality. They involve increases of 5 to 6 moles acid bound at acid pH, and 7 moles base bound at alkaline pH. They are associated with the irreversible denaturation of opsin in acid and alkaline solution, as evidenced by loss of its capacity to regenerate rhodopsin. Such frank denaturation procedures as the exposure of rhodopsin to alkali or heat in the dark result in comparable acid-base changes.

Entities:  

Keywords:  ACID-BASE EQUILIBRIUM; RHODOPSIN/physiology

Mesh:

Substances:

Year:  1956        PMID: 13346044      PMCID: PMC2147574          DOI: 10.1085/jgp.39.6.909

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  6 in total

1.  The sulfhydryl groups of crystalline proteins. I. Some albumins, enzymes, and hemoglobins.

Authors:  R E BENESCH; H A LARDY; R BENESCH
Journal:  J Biol Chem       Date:  1955-10       Impact factor: 5.157

2.  The cataphoretic mobility of visual purple.

Authors:  E E Broda; E Victor
Journal:  Biochem J       Date:  1940-12       Impact factor: 3.857

3.  The Visual Cycle and Protein Denaturation.

Authors:  A E Mirsky
Journal:  Proc Natl Acad Sci U S A       Date:  1936-02       Impact factor: 11.205

4.  The light reaction in the bleaching of rhodopsin.

Authors:  G WALD; J DURELL; C C ST GEORGE
Journal:  Science       Date:  1950-02-17       Impact factor: 47.728

5.  Cis-trans isomers of vitamin A and retinene in the rhodopsin system.

Authors:  R HUBBARD; G WALD
Journal:  J Gen Physiol       Date:  1952-11       Impact factor: 4.086

6.  The molar extinction of rhodopsin.

Authors:  G WALD; P K BROWN
Journal:  J Gen Physiol       Date:  1953-11-20       Impact factor: 4.086

  6 in total
  17 in total

1.  TAUTOMERIC FORMS OF METARHODOPSIN.

Authors:  R G MATTHEWS; R HUBBARD; P K BROWN; G WALD
Journal:  J Gen Physiol       Date:  1963-11       Impact factor: 4.086

2.  Binding of transducin and transducin-derived peptides to rhodopsin studies by attenuated total reflection-Fourier transform infrared difference spectroscopy.

Authors:  K Fahmy
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

3.  An analysis of light-induced admittance changes in rod outer segments.

Authors:  G Falk; P Fatt
Journal:  J Physiol       Date:  1973-02       Impact factor: 5.182

4.  Interaction between 6-hydroxydopamine and rhodopsin in vivo in the rat retina.

Authors:  S F Pong; L T Graham
Journal:  Experientia       Date:  1974-08-15

5.  Light-induced changes in the electrical impedance of the isolated frog retina.

Authors:  J A Coles
Journal:  J Physiol       Date:  1972-12       Impact factor: 5.182

6.  A charge transfer process in the visual pigments.

Authors:  I G Galindo
Journal:  Bull Math Biophys       Date:  1967-12

7.  Rapid hydrogen ion uptake of rod outer segments and rhodopsin solutions on illumination.

Authors:  G Falk; P Fatt
Journal:  J Physiol       Date:  1966-03       Impact factor: 5.182

8.  The C. elegans Taste Receptor Homolog LITE-1 Is a Photoreceptor.

Authors:  Jianke Gong; Yiyuan Yuan; Alex Ward; Lijun Kang; Bi Zhang; Zhiping Wu; Junmin Peng; Zhaoyang Feng; Jianfeng Liu; X Z Shawn Xu
Journal:  Cell       Date:  2016-11-17       Impact factor: 41.582

9.  The gecko visual pigment: a pH indicator with a salt effect.

Authors:  F Crescitelli
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

Review 10.  The ligand-binding domain of rhodopsin and other G protein-linked receptors.

Authors:  D D Oprian
Journal:  J Bioenerg Biomembr       Date:  1992-04       Impact factor: 2.945

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