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Chloride binding regulates the Schiff base pK in gecko P521 cone-type visual pigment.
- Source :
-
Biochemistry [Biochemistry] 1999 Apr 06; Vol. 38 (14), pp. 4649-54. - Publication Year :
- 1999
-
Abstract
- The binding of chloride is known to shift the absorption spectrum of most long-wavelength-absorbing cone-type visual pigments roughly 30 nm to the red. We determined that the chloride binding constant for this color shift in the gecko P521 visual pigment is 0.4 mM at pH 6.0. We found an additional effect of chloride on the P521 pigment: the apparent pKa of the Schiff base in P521 is greatly increased as the chloride concentration is increased. The apparent Schiff base pKa shifts from 8.4 for the chloride-free form to >10.4 for the chloride-bound form. We show that this shift is due to chloride binding to the pigment, not to the screening of the membrane surface charges by chloride ions. We also found that at high pH, the absorption maximum of the chloride-free pigment shifts from 495 to 475 nm. We suggest that the chloride-dependent shift of the apparent Schiff base pKa is due to the deprotonation of a residue in the chloride binding site with a pKa of ca. 8.5, roughly that of the Schiff base in the absence of chloride. The deprotonation of this site results in the formation of the 475 nm pigment and a 100-fold decrease in the pigment's ability to bind chloride. Increasing the concentration of chloride results in the stabilization of the protonated state of this residue in the chloride binding site and thus increased chloride binding with an accompanying increase in the Schiff base pK.
- Subjects :
- Animals
Binding Sites
Dose-Response Relationship, Drug
Hydrogen-Ion Concentration
Kinetics
Lizards
Photoreceptor Cells, Vertebrate chemistry
Photoreceptor Cells, Vertebrate metabolism
Protons
Retinal Cone Photoreceptor Cells chemistry
Rod Opsins chemistry
Schiff Bases metabolism
Spectrophotometry
Potassium Chloride metabolism
Retinal Cone Photoreceptor Cells metabolism
Rod Opsins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-2960
- Volume :
- 38
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 10194387
- Full Text :
- https://doi.org/10.1021/bi9828977