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PMID: 2573154 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Effect of carboxylic acid side chains on the absorption maximum of visual pigments.

Science (New York, N.Y.) ·Vol. 246 ·No. 4932 ·1989-11-17 ·Pages 928-30

Zhukovsky EA, Oprian DD

Abstract

The proposal that the absorption maximum of the visual pigments is governed by interaction of the 11-cis-retinal chromophore with charged carboxylic acid side chains in the membrane-embedded regions of the proteins has been tested by mutating five Asp and Glu residues thought to be buried in rhodopsin. Changing Glu113 to Gln causes a dramatic shift in the absorption maximum from 500 nanometers to 380 nanometers, a decrease in the pKa (acidity constant) of the protonated Schiff base of the chromophore to about 6, and a greatly increased reactivity with hydroxylamine. Thus Glu113 appears to be the counterion to the protonated Schiff base. Wavelength modulation in visual pigments apparently is not governed by electrostatic interaction with carboxylate residues, other than the counterion.

MeSH Terms
Aspartic Acid Glutamates Glutamic Acid Hydrogen-Ion Concentration Hydroxylamine Hydroxylamines/pharmacology Models, Molecular Mutation Protein Conformation Retinal Pigments/metabolism Retinaldehyde/metabolism Retinoids/metabolism Rhodopsin/genetics,metabolism Schiff Bases Spectrophotometry
Chemicals
Glutamates Hydroxylamines Retinal Pigments Retinoids Schiff Bases Hydroxylamine Aspartic Acid Glutamic Acid Rhodopsin Retinaldehyde
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zhukovsky E A
Department of Biochemistry, Brandeis University, Waltham, MA 02254.
Oprian D D
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1989-11-17
Pages
928-30
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NEI NIH HHS · R01 EY007965 · United States
NIGMS NIH HHS · 5T32 GM07596-11 · United States
NEI NIH HHS · EY07965 · United States
NCRR NIH HHS · S07 RR07044 · United States
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