Opsin Shifts in Bovine Rhodopsin and Bacteriorhodopsin. Comparison of Two External Point-Charge Models

Journal of the American Chemical Society

Volumn 102, Issue 27, 1980, Pages 7947-7949

  Motto, Michael G ^a   Sheves, Mordechai ^a   Tsujimoto, Kazuo ^a   Balogh Nair, Valeria ^a   Nakanishi, Koji ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33847086348     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00547a029     Document Type: Letter

References (20)

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2. Honig., B.; Dinur., U.; Nakanishi., K.; Balogh-Nair., V.; Gawinowicz., M. A.; Arnaboldi., M.; Motto., M. G. J. Am. Chem. Soc. 1979., 101., 7084.
3. Sec also: Arnaboldi., M.; Motto., M. G.; Tsujimoto., K.; Balogh-Nair., V.; Nakanishi., K. J. Am. Chem. Soc. 1979., 101., 7082. Sheves., M.; Nakanishi., K.; Honig., B. J. Am. Chem. Soc. 1979., 101., 7086.
4. Nakanishi., K.; Balogh-Nair., V.; Arnaboldi., M.; Tsujimoto., K.; Honig., B. J. Am. Chem. Soc., preceding paper.
5. Oesterhelt., D.; Stoeckenius., W. Nature (London) New Biol. 1971., 233., 149.
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7. Stoeckenius., W.; Lozier., R. H.; Bogomolni., R. A. Biochim. Biophys. Acta 1978., 505., 215.
8. The SBH+ theory is the one generally accepted., especially on grounds of resonance Raman studies: Callender., R.; Honig., B. Annu. Rev. Biophys. Bioeng. 1977., 6., 33. However., there is some controversy regarding the SBH+ theory. For leading references see: Favrot., J.; Leclercq., J. M.; Roberge., R.; Sandorfy., C.; Vocelle., D. Photochem. Photobiol. 1979., 29., 99. See also ref 5b.
9. Mayer., H.; Isler., O. In “Carotenoids”; Isler., O., Ed.; Birkhauser Verlag: Basel., 1971. Mayei,H. Pure Appl. Chem. 1979., 51., 535.
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12. Corey., E. J.; Venkateswarlu., A. J. Am. Chem. Soc. 1972., 94., 6190.
13. Analogous to the preparation of the corresponding α-ionyl compound: Barlett., L.; Klyne., W.; Mose., W. P.; Scopes., P. M.; Galsko., G.; Mallams., A. K.; Weedon., B. C. L.; Szabolcs., J.; Toth., G. J. Chem. Soc. C 1969., 2527.
14. Rambaud., R.; Vessiere., M. Bull. Soc. Chim. Fr. 1961., 1567.
15. In all incubation studies., a solution of the chromophore in ethanol was added to the deoxygenated opsin suspension; the final volume of ethanol was 1.0-2.0% of the incubation mixture: Matsumoto., H.; Horiuchi., K.; Yoshizawa., T. Biochim. Biophys. Acta 1978., 501., 257.
16. Bridges., C. D. B. Vision Res. 1977., 17., 301.
17. Kropf et al. have reported that an isomeric mixture of 9,13-demethyl analogue of 2 does not bind to bovine opsin: Kropf., A.; Whittenberger., B. P.; Goff., S. P.; Waggoner., A. S. Exp. Eye Res. 1973., 17., 591.
18. Hubbard., R.; Wald., G. J. Gen. Physiol. 1952., 36., 269. Wald., G.; Brown., P. K.; Hubbard., R.; Oroshnik., W. Proc. Natl. Acad. Sci. U.S.A. 1958., 41., 438. Hubbard., R.; Kropf., A. W. Proc. Natl. Acad. Sci. U.S.A. 1958., 44., 130.
19. The λmax values of SBH+ are measured in MeOH for the sake of simplicity because it has been shown that in this solvent the maxima are not affected by the counteranion: Erickson., J. O.; Blatz., P. E. Vision Res. 1968., 8., 1367.
20. Nelson., R.; DeRiel., J. K.; Kropf., A. Proc. Natl. Acad. Sci. U.S.A. 1970., 66., 531.