The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
IODOPSIN
Open accessAbstract
The iodopsin system found in the cones of the chicken retina is identical with the rhodopsin system in its carotenoids. It differs only in the protein—the opsin —with which carotenoid combines. The cone protein may be called photopsin to distinguish it from the scotopsins of the rods. Iodopsin bleaches in the light to a mixture of photopsin and all-trans retinene. The latter is reduced by alcohol dehydrogenase and cozymase to all-trans vitamin A1. Iodopsin is resynthesized from photopsin and a cis isomer of vitamin A, neovitamin Ab or the corresponding neoretinene b, the same isomer that forms rhodopsin. The synthesis of iodopsin from photopsin and neoretinene b is a spontaneous reaction. A second cis retinene, isoretinene a, forms iso-iodopsin (λmax 510 mµ). The bleaching of iodopsin in moderate light is a first-order reaction (Bliss). The synthesis of iodopsin from neoretinene b and opsin is second-order, like that of rhodopsin, but is very much more rapid. At 10°C. the velocity constant for iodopsin synthesis is 527 times that for rhodopsin synthesis. Whereas rhodopsin is reasonably stable in solution from pH 4–9, iodopsin is stable only at pH 5–7, and decays rapidly at more acid or alkaline reactions. The sulfhydryl poison, p-chloromercuribenzoate, blocks the synthesis of iodopsin, as of rhodopsin. It also bleaches iodopsin in concentrations which do not attack rhodopsin. Hydroxylamine also bleaches iodopsin, yet does not poison its synthesis. Hydroxylamine acts by competing with the opsins for retinene. It competes successfully with chicken, cattle, or frog scotopsin, and hence blocks rhodopsin synthesis; but it is less efficient than photopsin in trapping retinene, and hence does not block iodopsin synthesis. Though iodopsin has not yet been prepared in pure form, its absorption spectrum has been computed by two independent procedures. This exhibits an α-band with λmax 562 mµ, a minimum at about 435 mµ, and a small ß-band in the near ultraviolet at about 370 mµ. The low concentration of iodopsin in the cones explains to a first approximation their high threshold, and hence their status as organs of daylight vision. The relatively rapid synthesis of iodopsin compared with rhodopsin parallels the relatively rapid dark adaptation of cones compared with rods. A theoretical relation is derived which links the logarithm of the visual sensitivity with the concentration of visual pigment in the rods and cones. Plotted in these terms, the course of rod and cone dark adaptation resembles closely the synthesis of rhodopsin and iodopsin in solution. The spectral sensitivities of rod and cone vision, and hence the Purkinje phenomenon, have their source in the absorption spectra of rhodopsin and iodopsin. In the chicken, for which only rough spectral sensitivity measurements are available, this relation can be demonstrated only approximately. In the pigeon the scotopic sensitivity matches the spectrum of rhodopsin; but the photopic sensitivity is displaced toward the red, largely or wholly through the filtering action of the colored oil globules in the pigeon cones. In cats, guinea pigs, snakes, and frogs, in which no such colored ocular structures intervene, the scotopic and photopic sensitivities match quantitatively the absorption spectra of rhodopsin and iodopsin. In man the scotopic sensitivity matches the absorption spectrum of rhodopsin; but the photopic sensitivity, when not distorted by the yellow pigmentations of the lens and macula lutea, lies at shorter wave lengths than iodopsin. This discrepancy is expected, for the human photopic sensitivity represents a composite of at least three classes of cone concerned with color vision.
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Citations
Cites
Statistical Methods for Research Workers.
I., L., & Fisher, R. A. (1926) · Journal of the Royal Statistical Society · doi:10.2307/2341488 · Cited by 2,128
Wald, G. (1945) · Science · doi:10.1126/science.101.2635.653 · Cited by 615
Self-citationTHE MOLAR EXTINCTION OF RHODOPSIN
Wald, G., & Brown, P. K. (1953) · Journal of General Physiology · doi:10.1085/jgp.37.2.189 · Cited by 447
Self-citationCIS-TRANS ISOMERS OF VITAMIN A AND RETINENE IN THE RHODOPSIN SYSTEM
Hubbard, R., & Wald, G. (1952) · Journal of General Physiology · doi:10.1085/jgp.36.2.269 · Cited by 422
Self-citationTHE ROLE OF SULFHYDRYL GROUPS IN THE BLEACHING AND SYNTHESIS OF RHODOPSIN
Wald, G., & Brown, P. K. (1952) · Journal of General Physiology · doi:10.1085/jgp.35.5.797 · Cited by 210
Self-citationSensory Mechanisms of the Retina
(1947) · Postgraduate Medical Journal · doi:10.1136/pgmj.23.264.502-a · Cited by 210
The Light Reaction in the Bleaching of Rhodopsin
Wald, G., Durell, J., & St. George, R. C. C. (1950) · Science · doi:10.1126/science.111.2877.179 · Cited by 183
Self-citationWald, G. (1949) · Documenta Ophthalmologica · doi:10.1007/bf00162600 · Cited by 168
Self-citationPhoto-labile Pigments of the Chicken Retina
Wald, G. (1937) · Nature · doi:10.1038/140545a0 · Cited by 129
Self-citationCyanopsin, A New Pigment of Cone Vision
Wald, G., Brown, P. K., & Smith, P. H. (1953) · Science · doi:10.1126/science.118.3070.505 · Cited by 113
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Cited by
A novel multigene family may encode odorant receptors: A molecular basis for odor recognition
Buck, L., & Axel, R. (1991) · Cell · doi:10.1016/0092-8674(91)90418-x · Cited by 4,987
Spectral sensitivity of the foveal cone photopigments between 400 and 500 nm
Smith, V. C., & Pokorny, J. (1975) · Vision Research · doi:10.1016/0042-6989(75)90203-5 · Cited by 1,318
Molecular Basis of Visual Excitation
Wald, G. (1968) · Science · doi:10.1126/science.162.3850.230 · Cited by 832
Self-citationChemistry of Visual Adaptation in the Rat
DOWLING, J. E. (1960) · Nature · doi:10.1038/188114a0 · Cited by 543
THE BIOLOGICAL FUNCTION OF VITAMIN A ACID
Dowling, J. E., & Wald, G. (1960) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.46.5.587 · Cited by 451
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Metadata
- Authors
- Wald, G., Brown, P. K., & Smith, P. H.
- Venue
- The Journal of General Physiology
- Publisher
- Rockefeller University Press
- Published
- 1955-05-20
- Volume
- 38
- Issue
- 5
- Pages
- 623-681
- ISSN
- 0022-1295 (ISSN-L)
- 1540-7748
- OpenAlex
- W4231007405
- Cited by
- 325
- References
- 18
- FWCI
- 7.16
- Type
- journal article
- Language
- en
- Open access
- bronze
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