Cation Binding by Bacteriorhodopsin

• Published in: Proceedings of the National Academy of Sciences - PNAS 1985-01, Vol.82 (2), p.396-400
• Main Authors: C.-H. Chang, J.-G. Chen, Govindjee, R., Ebrey, T.
• Format: Article
• Language: English
• Subjects: Absorption spectra; bacteriorhodopsin; Bacteriorhodopsins; Binding sites; Biological and medical sciences; Biological Sciences: Biophysics; Calcium; Divalent cations; Fundamental and applied biological sciences. Psychology; Halobacterium salinarium; Interactions. Associations; Intermolecular phenomena; Magnesium; Molecular biophysics; P branes; Pigments; Protons; Purple membrane; purple membranes
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.82.2.396

We have found that extensively washed purple membrane has about 1 calcium and 3-4 magnesium ions bound per bacteriorhodopsin molecule. When these divalent cations are removed by any of a variety of means, the pigment changes its color from purple to blue (λmax≈ 600 nm). This blue pigment, which can be formed at near neutral pH, is probably very similar to blue species formed when the pH of a purple membrane sample is lowered to ≈ 2. When any of a wide variety of cations are added to a blue membrane preparation, the characteristic purple color of bacteriorhodopsin returns. Divalent and trivalent cations are much more efficient than monovalent cations in restoring the purple color and are effective at a ratio approaching one cation per pigment molecule. Besides shifting the absorption spectrum, removal of the divalent cations drastically alters the photochemical cycle of bacteriorhodopsin, including abolishing the unprotonated Schiff base (M-type) intermediate. Finally, lanthanum not only displaces the divalent cations normally bound to the purple membrane but also greatly reduces both the rate of decay of the M412 intermediate and proton uptake.