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PMID: 7272450 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Flash photolysis and low temperature photochemistry of bovine rhodopsin with a fixed 11-ene.

Biophysical journal ·Vol. 35 ·No. 2 ·1981-08-00 ·Pages 543-6

Mao B, Tsuda M, Ebrey TG, Akita H, Balogh-Nair V, Nakanishi K

Abstract

Nonbleachable rhodopsins containing retinal moieties with fixed 11-ene structures have been prepared. When the nonbleachable rhodopsin analogue corresponding to the natural pigment was flash-photolysed at 20.8 degrees C, no absorption changes occurred at the monitoring wavelengths of 380, 480, and 580 nm for the time range of 2 microseconds--10 s. This observation is in contrast to that of natural rhodopsin which showed the formation of metarhodopsin I and its decay to meta II. Irradiation of the artificial rhodopsin, 77 K, with light of 460 and 540 nm, also gave no spectral changes; in the case of natural rhodopsin, however, the irradiation leads to formation of the red-shifted intermediate bathorhodopsin. The absence of photochemistry in the artificial pigment shows that an 11-cis to trans photoisomerization of the retinal moiety is a crucial step in inducing the chain of events in te photolysis of rhodopsin.

MeSH Terms
Animals Cattle Freezing Kinetics Photochemistry Photolysis Retinal Pigments Rhodopsin Spectrophotometry
Chemicals
Retinal Pigments Rhodopsin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mao B
Tsuda M
Ebrey T G
Akita H
Balogh-Nair V
Nakanishi K
References (8)
8 references, click to expand
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1981-08-00
Pages
543-6
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1327542
Subset
IM
Grants
NEI NIH HHS · EY 01253 · United States
NEI NIH HHS · EY 01323 · United States
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