Abstract
Using rapid mixing techniques and resonance Raman spectroscopy, we have found that the 1H/2H exchange time for the Schiff base proton of bacteriorhodopsin in purple membrane is 4.7 msec, when experiments are carried out at pH 2 or pH 7 at room temperature in the dark. We argue that diffusion of neutral water into the membrane is fast on this time scale. Also, model Schiff bases in solution have a pKa between 6 and 7, and we show that such model Schiff bases have much faster exchange rates. Therefore, we conclude that the Schiff base proton in bacteriorhodopsin is protected from interaction with the medium, probably by interaction with a protein group, and this would account for a pKa considerably higher than 6-7.
MeSH Terms
Bacteriorhodopsins
Carotenoids
Halobacterium
Kinetics
Protons
Schiff Bases
Spectrum Analysis, Raman
Chemicals
Protons
Schiff Bases
Carotenoids
Bacteriorhodopsins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ehrenberg B
Lewis A
Porta T K
Nagle J F
Stoeckenius W
References (10)
10 references, click to expand
-
Bacteriorhodopsin and the purple membrane of halobacteria.
Biochim Biophys Acta. 1979 Mar 14;505(3-4):215-78
PMID: 35226
-
The pK of Schiff base deprotonation in bacteriorhodopsin.
Biochem Biophys Res Commun. 1978 Jun 29;82(4):1154-9
PMID: 29615
-
Light-dependent proton and rubidium translocation in membrane vesicles from Halobacterium halobium.
Biochem Biophys Res Commun. 1975 Jan 2;64(3):1054-61
PMID: 238520
-
Tunable laser resonance raman spectroscopy of bacteriorhodopsin.
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4462-6
PMID: 4530995
-
Functions of a new photoreceptor membrane.
Proc Natl Acad Sci U S A. 1973 Oct;70(10):2853-7
PMID: 4517939
-
Rhodopsin-like protein from the purple membrane of Halobacterium halobium.
Nat New Biol. 1971 Sep 29;233(39):149-52
PMID: 4940442
-
Reconstitution of purple membrane vesicles catalyzing light-driven proton uptake and adenosine triphosphate formation.
J Biol Chem. 1974 Jan 25;249(2):662-3
PMID: 4272126
-
Experimental evidence for secondary protein-chromophore interactions at the Schiff base linkage in bacteriorhodopsin: Molecular mechanism for proton pumping.
Proc Natl Acad Sci U S A. 1978 Oct;75(10):4642-6
PMID: 16592567
-
Molecular mechanisms for proton transport in membranes.
Proc Natl Acad Sci U S A. 1978 Jan;75(1):298-302
PMID: 272644
-
Kinetic resonance Raman spectroscopy: dynamics of deprotonation of the Schiff base of bacteriorhodopsin.
Science. 1977 Mar 25;195(4284):1328-30
PMID: 841330