SOLID-STATE C-13 AND N-15 NMR-STUDY OF THE LOW PH FORMS OF BACTERIORHODOPSIN

被引:124
作者
DEGROOT, HJM
SMITH, SO
COURTIN, J
VANDENBERG, E
WINKEL, C
LUGTENBURG, J
GRIFFIN, RG
HERZFELD, J
机构
[1] BRANDEIS UNIV, DEPT CHEM, WALTHAM, MA 02254 USA
[2] MIT, FRANCIS BITTER NATL MAGNET LAB, CAMBRIDGE, MA 02139 USA
[3] LEIDEN STATE UNIV, GORLAEUS LABS, 2300 RA LEIDEN, NETHERLANDS
关键词
D O I
10.1021/bi00481a017
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 visible absorption of bacteriorhodopsin (bR) is highly sensitive to pH, the maximum shifting from 568 nm (pH 7) to ~600 nm (pH 2) and back to 565 nm (pH 0) as the pH is decreased further with HC1. Blue membrane (λmax >600 nm) is also formed by deionization of neutral purple membrane suspensions. Low-temperature, magic angle spinning 13C and 15N NMR was used to investigate the transitions to the blue and acid purple states. The 15N NMR studies involved [∈-15N]lysine bR, allowing a detailed investigation of effects at the Schiff base nitrogen. The 15N resonance shifts ~ 16 ppm upfield in the neutral purple to blue transition and returns to its original value in the blue to acid purple transition. Thus, the 15N shift correlates directly with the color changes, suggesting an important contribution of the Schiff base counterion to the “opsin shift”. The results indicate weaker hydrogen bonding in the blue form than in the two purple forms and permit a determination of the contribution of the weak hydrogen bonding to the opsin shift at a neutral pH of ~2000 cm−1. An explanation of the mechanism of the purple to blue to purple transition is given in terms of the complex counterion model. The 13C NMR experiments were performed on samples specifically l3C labeled at the C-5, C-12, C-13, C-14, or C-15 positions in the retinylidene chromophore. The effects of the purple to blue to purple transitions on the isotropic chemical shifts for the various 13C resonances are relatively small. It appears that bR600 consists of at least four different species. The data confirm the presence of 13-cis- and all-trans-retinal in the blue form, as in neutral purple dark-adapted bR. All spectra of the blue and acid purple bR show substantial inhomogeneous broadening which indicates additional irregular distortions of the protein lattice. The amount of distortion correlates with the variation of the pH, and not with the color change. © 1990, American Chemical Society. All rights reserved.
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页码:6873 / 6883
页数:11
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