Volume and enthalpy changes in the early steps of bacteriorhodopsin photocycle studied by time-resolved photoacoustics

Biophysical Journal

Volumn 71, Issue 1, 1996, Pages 381-388

  Zhang, D ^a   Mauzerall, D ^a  

^a ROCKEFELLER UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 [(3 CHOLAMIDOPROPYL)DIMETHYLAMMONIO] 1 PROPANESULFONIC ACID; BACTERIORHODOPSIN; DEUTERIUM OXIDE; WATER;

ACOUSTICS; ARTICLE; ENERGY TRANSFER; ENTHALPY; HALOBACTERIUM SALINARUM; HYDROGEN BOND; NONHUMAN; PHOTOCHEMISTRY; PHOTOPERIODICITY; PROTEIN AGGREGATION; PURPLE MEMBRANE;

HALOBACTERIUM SALINARUM; MUS;

EID: 0029948137     PISSN: 00063495     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3495(96)79235-4     Document Type: Article

References (39)

1. Arnaut, L. G., R. A. Caldwell, J. E. Elbert, and L. A. Melton. 1992. Recent advances in photoacoustic calorimetry: theoretical basis and improvements in experimental design. Rev. Sci. Instrum. 63:5381-5389.
2. Ballard, S. G., and D. Mauzerall. 1980. Photochemical ionogenesis in solutions of zinc octacthylporphyrin. J. Chem. Phys. 72:933-947.
3. Birge, R. R., T. M. Cooper, A. F. Lawrence, M. B. Masthay, C. Zhang, and R. Zidovetzki. 1991. Revised assignment of energy storage in the primary photochemical event in Bacteriorhodopsin. J. Am. Chem. Soc. 113:4327-4328.
4. 1Bu*-like π, π* states. J. Chem. Phys. 92:7178-7195.
5. Braslavsky, S. E., and G. E. Heibel. 1992. Time-resolved photothermal and photoacoustic methods applied to photoinduced processes in solution. Chem. Rev. 92:1381-1410.
6. Dencher, N. A., K.-D. Kohl, and M. P. Heyn. 1983. Photochemical cycle and light-dark adaptation of monomeric and aggregated bacteriorhodopsin in various lipid environments. Biochemistry. 22:1323-1333.
7. Feitelson, J., and D. Mauzerall. 1993. Wide-band, time-resolved photoacoustic study of electron-transfer reactions: photoexcited magnesium porphyrin and quinones. J. Phys. Chem. 97:8410-8413.
8. Feitelson, J., and D. Mauzerall. 1996. Photoacoustic evolution of volume and entropy changes in energy and electron transfer. Triplet state porphyrin with oxygen and naphthoquinone-2-sulfonate. J. Phys. Chem. 100:7698-7703.
9. Govindjee, R., S. P. Balashov, and T. G. Ebrey. 1990. Quantum efficiency of the photochemical cycle of bacteriorhodopsin. Biophys. J. 58: 597-608.
10. Grzesiek, S., and N. A. Dencher. 1988. Monomeric and aggregated bacteriorhodopsin: single-turnover proton transport stoichiometry and photochemistry. Proc. Natl. Acad. Sci. USA. 85:9509-9513.
11. D96N. J. Phys. Chem. 96:4679-4685.
12. Henderson, R., and P. N. T. Unwin. 1975. Three-dimensional model of purple membrane obtained by electron microscopy. Nature. 257:28-32.
13. Hong, F. T. 1992. Bioelectrochemical processes in photobiological membranes. Biophys. Membr. Transp. 11:217-242.
14. Hong, F. T. 1994. Retinal proteins in photovoltaic devices. Adv. Chem. Ser. 240:527-59.
15. Kandori, H., Y. Yamazaki, J. Sasaki, R. Needleman, J. K. Lanyi, and A. Maeda. 1995. Water-mediated proton transfer in proteins: an FTIR study of bacteriorhodopsin. J. Am. Chem. Soc. 117:2118-2119.
16. Keszthelyi, L., and P. Ormos. 1980. Electric signals associated with the photocycle of bacteriorhodopsin. FEBS Lett. 109:189193.
17. Kono, M., and Ebrey, T. G. 1994. The K to L transiton of bacteriorhodopsin does not appear to be controlled by a proton transfer. Biophys. J. 66:A45.
18. Kubota, K., Y. Tominaga, S. Fujime, J. Otomo, and A. Ikegami. 1985. Dynamic light scattering study of suspensions of purple membrane. Biophys. Chem. 23:15-29.
19. Ley, A. C., and D. Mauzerall. 1982. Absolute absorption cross-sections for photosystem II and the minimum quantum requirement for photosynthesis in the Chlorella vulgaris. Biochim. Biophys. Acta. 680:174-180.
20. Malkin, S., M. S. Churio, S. Shocjat, and S. E. Braslavsky. 1994. Photochemical energy storage and volume changes in the microsecond time range in bacterial photosynthesis a laser induced optoacoustic study. J. Photochem. Photobiol. B. Biol. 23:79-85.
21. Marinetti, T. 1988. Nonproton ion release by purple membranes exhibits cooperativity as shown by determination of the optical cross-section. Biophys. J. 54:197-204.
22. Mauzerall, D. 1982. Statistical theory of the effect of multiple excitation in photosynthetic systems. In Biological events probed by ultrafast laser spectroscopy. R. R. Alfano, editor. Academic Press, New York. 215-235.
23. Mauzerall, D., M. R. Gunner, and J. W. Zhang. 1995. Volume contraction on photoexcitation of the reaction center from rhodobacler sphaeroides R-26: internal probe of dielectrics. Biophys. J. 68:275-280.
24. Nagle, J. F., S. M. Bhattacharjee, L. A. Parodi, and R. H. Lozier. 1983. Effect of photoselection upon saturation and the dichroic ratio in flash experiments upon effectively immobilized systems. Photochem. Photobiol. 38:331-339.
25. Norris, C. L., and K. S. Peters. 1993. A photoacoustic calorimetry study of horse carboxymyoglobin on the 10-nanosecond time scale. Biophys. J. 65:1660-1665.
26. Oesterhelt, D., and W. Stoeckenius. 1974. Isolation of the cell membrane of Halobacterium halobium and its fractionation into red and purple membrane. Methods Enzymol. 31A:667-678.
27. Oesterhelt, D., and J. Tittor. 1989. Two pumps, one principle: light-driven ion transport in Halobacteria. Trends Biochem. Sci. 14:57-61.
28. Polland, H. J., M. A. Franz, W. Zinth, W. Kaiser, and D. Oesterhelt. 1986. Energy transfer from retinal to amino acids - a time-resolved study of the ultraviolet emission of bacteriorhodopsin. Biochim. Biophys. Acta. 851:407-415.
29. Rees, D. C., A. J. Chirino, K. H. Kim, and H. Komiya. 1994. Membrane protein structure and stability: implications of the first crystallographic analyses. Methods Physiol. Ser. 1:3-26.
30. Rhor, M., W. Gartner, G. Schweitzer, A. R. Holzwarth, and S. E. Braslavsky. 1992. Quantum yields of the photochromic equilibrium between Bacteriorhodopsin and its bathointermediate K. Femto- and nanosecond optoacoustic spectroscopy. J. Phys. Chem. 96:6055-6061.
31. Schulenberg, P. J., W. Gartner, and S. E. Braslavsky. 1995. Time-resolved volume changes during the Bacteriorhodopsin photocycle: a photothermal beam deflection study. J. Phys. Chem. 99:9617-9624.
32. Schulenberg, P. J., M. Rohr, W. Gartner, and S. E. Braslavsky. 1994. Photoinduced volume changes associated with the early transformation of bacteriorhodopsin: a laser-induced optoacoustic spectroscopy study. Biophys. J. 66:838-843.
33. Siebert, F., and W. Mantele. 1983. Investigation of the primary photochemistry of Bacteriorhodopsin by low temperature Fourier transform infrared spectroscopy. Eur. J. Biochem. 130:565-573.
34. Stoeckenius, W., R. H. Lozier, and R. A. Bogomolni. 1979. Bacteriorhodopsin and the purple membrane of halobacteria. Biochim. Biophys. Acta. 505:215-278.
35. Trissl, H.-W. 1990. Photoelectric measurements of purple membranes. Photochem. Photobiol. 51:793-818.
36. Varo, G., and K. Lanyi. 1991. Thermodynamics and energy coupling in the bacteriorhodopsin photocycle. Biochemistry. 30:5016-5022.
37. Varo, G., and K. Lanyi. 1995. Effects of hydrostatic pressure on the kinetics reveal a volume increase during the Bacteriorhodopsin photocycle. Biochemistry. 34:12161-12169.
38. Westrick, J. A., J. L. Goodman, and K. S. Peters. 1987. A time-resolved photoacoustic calorimetry study of the dynamics of enthalpy and volume changes produced in the photodissociation of carbon monoxide from sperm whale carboxymyoglobin. Biochemistry. 29:6741-6746.
39. Xie, A. H., J. F. Nagle, and R. H. Lozier. 1987. Flash spectroscopy of purple membrane. Biophys. J. 51:627-635.