Morphology of three lyotropic liquid crystalline biological NMR media studied by translational diffusion anisotropy

被引:127
作者
Gaemers, S [1 ]
Bax, A [1 ]
机构
[1] NIDDKD, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1021/ja011967l
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The morphologies of three dilute liquid crystalline phases, which are widely used for biological NMR spectroscopy, are investigated by the study of tracer self-diffusion. The aqueous liquid crystalline media investigated include the common phospholipid bicelle medium, a phase consisting of a mixture of pentaethyleneglycol mono dodecyl ether and hexanol, and a medium containing cetylpyridinium bromide and hexanol. Threonine and water were used as tracer molecules for probing the aqueous environment, and tetramethylsilane (TMS) was for probing the lipophilic environment. Pulsed field gradient NMR was used to measure tracer self-diffusion rates in three orthogonal directions. Although results for the water-soluble tracers in bicelle media do not contradict the widely accepted disk-shaped bicelle model, the high TMS diffusion rate observed in the bilayer plane requires extensive transient edge-to-edge contacts of such disks. This morphology is essentially that of a heavily perforated lamellar bilayer phase and explains why this medium remains liquid crystalline well below the Onsager limit for disk-shaped nematogens. Below 25 degreesC, a bicelle mixture consisting of dimyristoyl phosphatidyl choline and dihexanoyl phosphatidyl choline remains isotropic, but tracer diffusion obstruction indicates that the particles are significantly oblate. The diffusion anisotropy in the penta(ethyleneglycol) mono dodecyl ether liquid crystals confirms the previously proposed alpha -lamellar phase. However, weak inhibition of aqueous-phase self-diffusion in the z direction points to the presence of bridge- or caplike obstructions, and the bilayers appear slightly permeable to water. If the previously proposed concentric cylinder superstructure of bilayers applies, the diffusion data indicate that the most outer cylinder must have a diameter greater than 50 mum. The tracer self-diffusion data for the cetylpyridinium bromide/hexanol medium is only compatible with a planar alpha -lamellar phase, with its local director orthogonal to the magnetic field, and a very large domain size over which the director remains parallel.
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收藏
页码:12343 / 12352
页数:10
相关论文
共 80 条
[1]   ASSOCIATION OF BIOMOLECULAR SYSTEMS VIA PULSED-FIELD GRADIENT NMR SELF-DIFFUSION MEASUREMENTS [J].
ALTIERI, AS ;
HINTON, DP ;
BYRD, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (28) :7566-7567
[2]   Recognition of protein folds via dipolar couplings [J].
Annila, A ;
Aitio, H ;
Thulin, E ;
Drakenberg, T .
JOURNAL OF BIOMOLECULAR NMR, 1999, 14 (03) :223-230
[3]   Characterization of surfactant liquid crystal phases suitable for molecular alignment and measurement of dipolar couplings [J].
Barrientos, LG ;
Dolan, C ;
Gronenborn, AM .
JOURNAL OF BIOMOLECULAR NMR, 2000, 16 (04) :329-337
[4]   High-resolution heteronuclear NMR of human ubiquitin in an aqueous liquid crystalline medium [J].
Bax, A ;
Tjandra, N .
JOURNAL OF BIOMOLECULAR NMR, 1997, 10 (03) :289-292
[5]   Solution structure of cyanovirin-N, a potent HIV-inactivating protein [J].
Bewley, CA ;
Gustafson, KR ;
Boyd, MR ;
Covell, DG ;
Bax, A ;
Clore, GM ;
Gronenborn, AM .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (07) :571-578
[6]  
BOTHNERBY AA, 1996, ENCY NUCL MAGNETIC R, V5, P2932
[7]   A proton nuclear magnetic resonance relaxation study of C12E6/D2O [J].
Burnell, EE ;
Capitani, D ;
Casieri, C ;
Segre, AL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (37) :8782-8791
[8]   EXAMINATION OF THE LAMELLAR PHASE OF AEROSOL OT-WATER USING PULSED FIELD GRADIENT NUCLEAR MAGNETIC-RESONANCE [J].
CALLAGHAN, PT ;
SODERMAN, O .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (10) :1737-1744
[9]  
CANTOR CR, 1980, BIOPHYSICAL CHEM 2
[10]   Improved low pH bicelle system for orienting macromolecules over a wide temperature range [J].
Cavagnero, S ;
Dyson, HJ ;
Wright, PE .
JOURNAL OF BIOMOLECULAR NMR, 1999, 13 (04) :387-391