Purple membrane lipid control of bacteriorhodopsin conformational flexibility and photocycle activity. An infrared spectroscopic study

التفاصيل البيبلوغرافية
العنوان: Purple membrane lipid control of bacteriorhodopsin conformational flexibility and photocycle activity. An infrared spectroscopic study
المؤلفون: Salil Bose, Steven M. Barnett, Richard W. Hendler, Ira W. Levin, Swetlana Dracheva
المصدر: European Journal of Biochemistry. 270:1920-1925
بيانات النشر: Wiley, 2003.
سنة النشر: 2003
مصطلحات موضوعية: biology, Chemistry, Membrane lipids, Bacteriorhodopsin, Halobacterium, biology.organism_classification, Biochemistry, Transmembrane protein, Crystallography, Transmembrane domain, Membrane, Protein structure, Biophysics, biology.protein, Bacteriorhodopsins
الوصف: Specific lipids of the purple membrane of Halobacteria are required for normal bacteriorhodopsin structure, function, and photocycle kinetics [Hendler, R.W. & Dracheva, S. (2001) Biochemistry (Moscow)66, 1623-1627]. The decay of the M-fast intermediate through a path including the O intermediate requires the presence of a hydrophobic environment near four charged aspartic acid residues within the cytoplasmic loop region of the protein (R. W. Hendler & S. Bose, unpublished results). On the basis of the unique ability of squalene, the most hydrophobic purple membrane lipid, to induce recovery of M-fast activity in Triton-treated purple membrane, we proposed that this uncharged lipid modulates an electrostatic repulsion between the membrane surface of the inner trimer space and the nearby charged aspartic acids of the cytoplasmic loop region to promote transmembrane alpha-helical mobility with a concomitant increase in the speed of the photocycle. We examined Triton-treated purple membranes in various stages of reconstitution with native lipid suspensions using infrared spectroscopic techniques. We demonstrate a correlation between the vibrational half-width parameter of the protein alpha-helical amide I mode at 1660 cm-1, reflecting the motional characteristics of the transmembrane helices, and the lipid-induced recovery of native bacteriorhodopsin properties in terms of the visible absorbance maxima of ground state bacteriorhodopsin and the mean decay times of the photocycle M-state intermediates.
تدمد: 1432-1033
0014-2956
1623-1627
DOI: 10.1046/j.1432-1033.2003.03547.x
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c2308c83519af99486f95ac7d169ecec
https://doi.org/10.1046/j.1432-1033.2003.03547.x
Rights: OPEN
رقم الانضمام: edsair.doi...........c2308c83519af99486f95ac7d169ecec
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14321033
00142956
16231627
DOI:10.1046/j.1432-1033.2003.03547.x