Tyrosine and carboxyl protonation changes in the bacteriorhodopsin photocycle. 2. Tyrosine-26 and -64
Journal Article
·
· Biochemistry; (United States)
Low-temperature Fourier transform infrared (FTIR) and UV difference spectroscopies combined with selective tyrosine nitration and tyrosine isotopic labeling have been used to investigate the participation of tyrosines-26 and -64 in the bacteriorhodopsin (bR) photocycle. Nitration of Tyr-26 has no detectable effect on the FTIR or UV difference spectra of the BR/sub 570/ ..-->.. K/sub 630/ or BR/sub 570/ ..-->.. M/sub 412/ transitions. In contrast, nitration of Tyr-64 causes changes in both the FTIR and UV spectra of these transitions. However, this nitration does not alter tyrosine peaks in the FTIR difference spectra which have previously been associated with the protonation of a tyrosinate by K/sub 630/ and the deprotonation of a tyrosine by M/sub 412/. Instead, Tyr-64 nitration appears to affect other tyrosine peaks. These results and changes in UV difference spectra upon Tyr-64 nitration are consistent with the deprotonation of Tyr-64 by M/sub 412/ as concluded previously. Effects on chromophore vibrations caused by Tyr-64 nitration are unaltered upon reducing the nitrotyrosine to aminotyrosine with sodium dithionite. Finally, nitro-Tyr-64 causes a shift in the frequency of a positive peak at 1739 cm/sup -1/ in the BR/sub 570/ ..-->.. M/sub 412/ FTIR difference spectrum which reflects the protonation of a carboxyl-containing residue. The shift does not occur for samples containing amino-Tyr-64. These data suggest that Tyr-64 may interact with this carboxyl group.
- Research Organization:
- Boston Univ., MA
- OSTI ID:
- 5532174
- Journal Information:
- Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 26:21; ISSN BICHA
- Country of Publication:
- United States
- Language:
- English
Similar Records
Tyrosine and carboxyl protonation changes in the bacteriorhodopsin photocycle. 1. M/sub 412/ and L/sub 550/ intermediates
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Journal Article
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Tue Oct 20 00:00:00 EDT 1987
· Biochemistry; (United States)
·
OSTI ID:5658009
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Journal Article
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Mon Dec 16 23:00:00 EST 1985
· Biochemistry; (United States)
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OSTI ID:5776463
Deprotonation of tyrosines in bacteriorhodopsin as studies by Fourier transform infrared spectroscopy with deuterium and nitrate labeling
Journal Article
·
Mon Dec 14 23:00:00 EST 1987
· Biochemistry; (United States)
·
OSTI ID:5303899
Related Subjects
14 SOLAR ENERGY
140505* -- Solar Energy Conversion-- Photochemical
Photobiological
& Thermochemical Conversion-- (1980-)
550201 -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AMINO ACIDS
BIOCHEMISTRY
CARBOXYLIC ACIDS
CHEMICAL SHIFT
CHEMISTRY
DEUTERIUM COMPOUNDS
HYDROGEN COMPOUNDS
HYDROXY ACIDS
INFRARED SPECTRA
MEMBRANES
ORGANIC ACIDS
ORGANIC COMPOUNDS
PHOTOCHEMISTRY
PHOTOSYNTHETIC BACTERIA
PHOTOSYNTHETIC MEMBRANES
PIGMENTS
PROTEINS
RHODOPSIN
SPECTRA
TYROSINE
ULTRAVIOLET SPECTRA
140505* -- Solar Energy Conversion-- Photochemical
Photobiological
& Thermochemical Conversion-- (1980-)
550201 -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AMINO ACIDS
BIOCHEMISTRY
CARBOXYLIC ACIDS
CHEMICAL SHIFT
CHEMISTRY
DEUTERIUM COMPOUNDS
HYDROGEN COMPOUNDS
HYDROXY ACIDS
INFRARED SPECTRA
MEMBRANES
ORGANIC ACIDS
ORGANIC COMPOUNDS
PHOTOCHEMISTRY
PHOTOSYNTHETIC BACTERIA
PHOTOSYNTHETIC MEMBRANES
PIGMENTS
PROTEINS
RHODOPSIN
SPECTRA
TYROSINE
ULTRAVIOLET SPECTRA