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The thermal contribution to photoactivation in A2 visual pigments studied by temperature effects on spectral properties

Published online by Cambridge University Press:  18 November 2003

PETRI ALA-LAURILA
Affiliation:
Laboratory of Biomedical Engineering, Helsinki University of Technology, FIN-02015 HUT, Finland
RAULI-JAN ALBERT
Affiliation:
Laboratory of Biomedical Engineering, Helsinki University of Technology, FIN-02015 HUT, Finland
PIA SAARINEN
Affiliation:
Department of Biosciences, Division of Animal Physiology, FIN-00014 University of Helsinki, Finland
ARI KOSKELAINEN
Affiliation:
Laboratory of Biomedical Engineering, Helsinki University of Technology, FIN-02015 HUT, Finland
KRISTIAN DONNER
Affiliation:
Department of Biosciences, Division of Animal Physiology, FIN-00014 University of Helsinki, Finland

Abstract

Effects of temperature on the spectral properties of visual pigments were measured in the physiological range (5–28°C) in photoreceptor cells of bullfrog (Rana catesbeiana) and crucian carp (Carassius carassius). Absorbance spectra recorded by microspectrophotometry (MSP) in single cells and sensitivity spectra recorded by electroretinography (ERG) across the isolated retina were combined to yield accurate composite spectra from ca. 400 nm to 800 nm. The four photoreceptor types selected for study allowed three comparisons illuminating the properties of pigments using the dehydroretinal (A2) chromophore: (1) the two members of an A1/A2 pigment pair with the same opsin (porphyropsin vs. rhodopsin in bullfrog “red” rods); (2) two A2 pigments with similar spectra (porphyropsin rods of bullfrog and crucian carp); and (3) two A2 pigments with different spectra (rods vs. long-wavelength-sensitive (L-) cones of crucian carp). Qualitatively, the temperature effects on A2 pigments were similar to those described previously for the A1 pigment of toad “red” rods. Warming caused an increase in relative sensitivities at very long wavelengths but additionally a small shift of λmax toward shorter wavelengths. The former effect was used for estimating the minimum energy required for photoactivation (Ea) of the pigment. Bullfrog rod opsin with A2 chromophore had Ea = 44.2 ± 0.9 kcal/mol, significantly lower (one-tailed P < 0.05) than the value Ea = 46.5 ± 0.8 kcal/mol for the same opsin coupled to A1. The A2 rod pigment of crucian carp had Ea = 42.3 ± 0.6 kcal/mol, which is significantly higher (one-tailed P < 0.01) than that of the L-cones in the same retina (Ea = 38.3 ± 0.4 kcal/mol), whereas the difference compared with the bullfrog A2 rod pigment is not statistically significant (two-tailed P = 0.13). No strict connection between λmax and Ea appears to exist among A2 pigments any more than among A1 pigments. Still, the A1 → A2 chromophore substitution in bullfrog opsin causes three changes correlated as originally hypothesized by Barlow (1957): a red-shift of λmax, a decrease in Ea, and an increase in thermal noise.

Type
Research Article
Copyright
2003 Cambridge University Press

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