Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1987 Jun;51(6):875–881. doi: 10.1016/S0006-3495(87)83415-X

Abrupt onset of large scale nonproton ion release in purple membranes caused by increasing pH or ionic strength.

T Marinetti
PMCID: PMC1330021  PMID: 3607209

Abstract

The abrupt onset of large scale nonproton ion release by photo-excited purple membrane suspensions has been observed near neutral pH using transient conductivity measurements. At pH 7 and low ionic strength, the conductivity transients due to proton and nonproton ions are of comparable magnitude but of opposite sign: fast proton release and ion uptake, followed by slow proton uptake and ion release. By increasing either the pH or the NaCl concentration, the amplitude of the conductivity transient increases sharply and the signal is then dominated by nonproton ion release. These results can be understood in terms of light-induced changes in the population of counterions condensed at the purple membrane surface caused by changes in the surface charge density. The critical charge density required for condensation to occur is evidently achieved near neutral pH by ionizing dissociable groups on the membrane by either titration (increasing the pH) or shifting their pKs (increasing the ionic strength).

Full text

PDF
875

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ahl P. L., Cone R. A. Light activates rotations of bacteriorhodopsin in the purple membrane. Biophys J. 1984 Jun;45(6):1039–1049. doi: 10.1016/S0006-3495(84)84251-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dencher N., Wilms M. Flash photometric experiments on the photochemical cycle of bacteriorhodopsin. Biophys Struct Mech. 1975 May 30;1(3):259–271. doi: 10.1007/BF00535760. [DOI] [PubMed] [Google Scholar]
  3. Draheim J. E., Cassim J. Y. Large Scale Global Structural Changes of the Purple Membrane during the Photocycle. Biophys J. 1985 Apr;47(4):497–507. doi: 10.1016/S0006-3495(85)83943-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Fisher K. A., Yanagimoto K., Stoeckenius W. Oriented adsorption of purple membrane to cationic surfaces. J Cell Biol. 1978 May;77(2):611–621. doi: 10.1083/jcb.77.2.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Frankel R. D., Forsyth J. M. Time-resolved x-ray diffraction study of photostimulated purple membrane. Biophys J. 1985 Mar;47(3):387–393. doi: 10.1016/S0006-3495(85)83930-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Garty H., Klemperer G., Eisenbach M., Caplan S. R. The direction of light-induced pH changes in purple membrane suspensions. Influence of pH and temperature. FEBS Lett. 1977 Sep 15;81(2):238–242. doi: 10.1016/0014-5793(77)80526-7. [DOI] [PubMed] [Google Scholar]
  7. Glaeser R. M., Baldwin J., Ceska T. A., Henderson R. Electron diffraction analysis of the M412 intermediate of bacteriorhodopsin. Biophys J. 1986 Nov;50(5):913–920. doi: 10.1016/S0006-3495(86)83532-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Govindjee R., Ebrey T. G., Crofts A. R. The quantum efficiency of proton pumping by the purple membrane of Halobacterium halobium. Biophys J. 1980 May;30(2):231–242. doi: 10.1016/S0006-3495(80)85091-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Henderson R., Jubb J. S., Whytock S. Specific labelling of the protein and lipid on the extracellular surface of purple membrane. J Mol Biol. 1978 Aug 5;123(2):259–274. doi: 10.1016/0022-2836(78)90325-x. [DOI] [PubMed] [Google Scholar]
  10. Henderson R. The purple membrane from Halobacterium halobium. Annu Rev Biophys Bioeng. 1977;6:87–109. doi: 10.1146/annurev.bb.06.060177.000511. [DOI] [PubMed] [Google Scholar]
  11. Kushwaha S. C., Kates M., Stoeckenius W. Comparison of purple membrane from Halobacterium cutirubrum and Halobacterium halabium. Biochim Biophys Acta. 1976 Apr 5;426(4):703–710. doi: 10.1016/0005-2736(76)90135-8. [DOI] [PubMed] [Google Scholar]
  12. Lozier R. H., Niederberger W., Bogomolni R. A., Hwang S., Stoeckenius W. Kinetics and stoichiometry of light-induced proton release and uptake from purple membrane fragments, Halobacterium halobium cell envelopes, and phospholipid vesicles containing oriented purple membrane. Biochim Biophys Acta. 1976 Sep 13;440(3):545–556. doi: 10.1016/0005-2728(76)90041-4. [DOI] [PubMed] [Google Scholar]
  13. MacDonald R. C., Simon S. A., Baer E. Ionic influences on the phase transition of dipalmitoylphosphatidylserine. Biochemistry. 1976 Feb 24;15(4):885–891. doi: 10.1021/bi00649a025. [DOI] [PubMed] [Google Scholar]
  14. Manning G. S. The molecular theory of polyelectrolyte solutions with applications to the electrostatic properties of polynucleotides. Q Rev Biophys. 1978 May;11(2):179–246. doi: 10.1017/s0033583500002031. [DOI] [PubMed] [Google Scholar]
  15. Marinetti T., Mauzerall D. Absolute quantum yields and proof of proton and nonproton transient release and uptake in photoexcited bacteriorhodopsin. Proc Natl Acad Sci U S A. 1983 Jan;80(1):178–180. doi: 10.1073/pnas.80.1.178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Marinetti T., Mauzerall D. Large transient nonproton ion movements in purple membrane suspensions are abolished by solubilization in Triton X-100. Biophys J. 1986 Sep;50(3):405–415. doi: 10.1016/S0006-3495(86)83476-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. McDiarmid R., Doty P. The spectrophotometric titration of polyacrylic, poly-L-aspartic, and poly-L-glutamic acids. J Phys Chem. 1966 Aug;70(8):2620–2627. doi: 10.1021/j100880a030. [DOI] [PubMed] [Google Scholar]
  18. Mitchell D., Rayfield G. W. Order of proton uptake and release by bacteriorhodopsin at low pH. Biophys J. 1986 Feb;49(2):563–566. doi: 10.1016/S0006-3495(86)83666-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Neugebauer D. C., Oesterhelt D., Zingsheim H. P. The two faces of the purple membrane. II. Differences in surface charge properties revealed by ferritin binding. J Mol Biol. 1978 Oct 25;125(2):123–135. doi: 10.1016/0022-2836(78)90341-8. [DOI] [PubMed] [Google Scholar]
  20. Oesterhelt D., Stoeckenius W. Functions of a new photoreceptor membrane. Proc Natl Acad Sci U S A. 1973 Oct;70(10):2853–2857. doi: 10.1073/pnas.70.10.2853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Oesterhelt D., Stoeckenius W. Isolation of the cell membrane of Halobacterium halobium and its fractionation into red and purple membrane. Methods Enzymol. 1974;31:667–678. doi: 10.1016/0076-6879(74)31072-5. [DOI] [PubMed] [Google Scholar]
  22. Ort D. R., Parson W. W. Enthalpy changes during the photochemical cycle of bacteriorhodopsin. Biophys J. 1979 Feb;25(2 Pt 1):355–364. doi: 10.1016/s0006-3495(79)85297-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ort D. R., Parson W. W. Flash-induced volume changes of bacteriorhodopsin-containing membrane fragments and their relationship to proton movements and absorbance transients. J Biol Chem. 1978 Sep 10;253(17):6158–6164. [PubMed] [Google Scholar]
  24. Ort D. R., Parson W. W. The quantum yield of flash-induced proton release by bacteriorhodopsin-containing membrane fragments. Biophys J. 1979 Feb;25(2 Pt 1):341–353. doi: 10.1016/s0006-3495(79)85296-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Otomo J., Ohno K., Takeuchi Y., Ikegami A. Surface charge movements of purple membrane during light-dark adaptation. Biophys J. 1986 Aug;50(2):205–211. doi: 10.1016/S0006-3495(86)83454-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Renthal R., Cha C. H. Charge asymmetry of the purple membrane measured by uranyl quenching of dansyl fluorescence. Biophys J. 1984 May;45(5):1001–1006. doi: 10.1016/S0006-3495(84)84245-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Slifkin M. A., Garty H., Sherman W. V., Vincent M. F., Caplan S. R. Light-induced conductivity changes in purple membrane suspensions. Biophys Struct Mech. 1979 Aug;5(4):313–320. doi: 10.1007/BF02426665. [DOI] [PubMed] [Google Scholar]
  28. Stoeckenius W., Bogomolni R. A. Bacteriorhodopsin and related pigments of halobacteria. Annu Rev Biochem. 1982;51:587–616. doi: 10.1146/annurev.bi.51.070182.003103. [DOI] [PubMed] [Google Scholar]
  29. Stoeckenius W., Lozier R. H., Bogomolni R. A. Bacteriorhodopsin and the purple membrane of halobacteria. Biochim Biophys Acta. 1979 Mar 14;505(3-4):215–278. doi: 10.1016/0304-4173(79)90006-5. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES