Modulation of the metarhodopsin I/metarhodopsin II equilibrium of bovine rhodopsin by ionic strength - Evidence for a surface-charge effect
被引:37
作者:
DeLange, F
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机构:Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
DeLange, F
Merkx, M
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机构:Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
Merkx, M
BoveeGeurts, PHM
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机构:Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
BoveeGeurts, PHM
Pistorius, AMA
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机构:Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
Pistorius, AMA
DeGrip, W
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机构:Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
DeGrip, W
机构:
[1] Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen
[2] Dept. of Biochemistry F.M.W.-160, Institute of Cellular Signalling, University of Nijmegen, NL-6500 HB Nijmegen
来源:
EUROPEAN JOURNAL OF BIOCHEMISTRY
|
1997年
/
243卷
/
1-2期
关键词:
bovine rhodopsin;
metarhodopsin I metarhodopsin II equilibrium;
pK(a);
ionic strength;
surface charge;
D O I:
10.1111/j.1432-1033.1997.0174a.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The effects of ionic strength on formation and decay of metarhodopsin II (MII), the active photointermediate of bovine rhodopsin, were studied in the native membrane environment by means of ultraviolet/visible and Fourier-transform infrared (FTIR) spectroscopy. By increasing the concentration of KCl in the range from hypotonic to 4 M, the apparent pK(a) of the metarhodopsin I(MI)/MII equilibrium is shifted by approximately pH three, in favor of the MII intermediate. In addition, the apparent rate of MII formation is enhanced by an increase in ionic strength (about twofold in the presence of 2 M KCl). MII decay is independent of the salt concentration. Attenuated-total-reflectance/FTIR data show that the high-salt conditions have no effect on the rigidity of the membrane matrix and do not induce: structural changes in the intermediates themselves. Different salts were tested for their ability to shift the MI/MII equilibrium; however, no clear ion dependence was observed. We interpret these results as an indication for direct involvement of the cytosolic surface charge in the regulation of the photochemical activity of bovine rhodopsin.