Characterization of magnetically oriented phospholipid micelles for measurement of dipolar couplings in macromolecules

被引:225
作者
Ottiger, M [1 ]
Bax, A [1 ]
机构
[1] NIDDKD, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
alignment; bicelle; dipolar coupling; liquid crystal; protein NMR; phospholipid;
D O I
10.1023/A:1008366116644
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
Weak alignment of solute molecules with the magnetic field can be achieved in a dilute liquid crystalline medium, consisting of an aqueous mixture of dimyristoyl-phosphatidylcholine (DMPC) and dihexanoyl-phosphatidylcholine (DHPC). For a certain range of molar ratios, DMPC and DHPC can form large, disc-shaped particles, commonly referred to as bicelles (Sanders and Schwonek, 1992), which cooperatively align in the magnetic field and induce a small degree of alignment on asymmetrically shaped solute molecules. As a result, dipolar couplings between pairs of H-1, C-13 or N-15 nuclei are no longer averaged to zero by rotational diffusion and they can be readily measured, providing valuable structural information. The stability of these liquid crystals and the degree of alignment of the solute molecules depend strongly on experimental variables such as the DMPC:DHPC ratio and concentration, the preparation protocol of the DMPC/DHPC mixtures, as well as salt, temperature, and pH. The lower temperature limit for which the liquid crystalline phase is stable can be reduced to 20 degrees C by using a ternary mixture of DHPC, DMPC, and 1-myristoyl-2-myristoleoyl-sn-glycero-3-phosphocholine, or a binary mixture of DHPC and ditridecanoyl-phosphatidylcholine. These issues are discussed, with an emphasis on the use of the medium for obtaining weak alignment of biological macromolecules.
引用
收藏
页码:361 / 372
页数:12
相关论文
共 35 条
[1]  
Bastiaan E. W., 1987, ANNU REP NMR SPECTRO, V19, P35
[2]   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
[3]  
Bothner-By A. A., 1996, ENCY NUCL MAGNETIC R, P2932
[4]   MONOMER-TO-MICELLE TRANSITION OF DIHEXANOYLPHOSPHATIDYLCHOLINE - C-13 NMR AND RAMAN STUDIES [J].
BURNS, RA ;
ROBERTS, MF ;
DLUHY, R ;
MENDELSOHN, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (02) :430-438
[5]   A robust method for determining the magnitude of the fully asymmetric alignment tensor of oriented macromolecules in the absence of structural information [J].
Clore, GM ;
Gronenborn, AM ;
Bax, A .
JOURNAL OF MAGNETIC RESONANCE, 1998, 133 (01) :216-221
[6]   NMRPIPE - A MULTIDIMENSIONAL SPECTRAL PROCESSING SYSTEM BASED ON UNIX PIPES [J].
DELAGLIO, F ;
GRZESIEK, S ;
VUISTER, GW ;
ZHU, G ;
PFEIFER, J ;
BAX, A .
JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (03) :277-293
[7]   PHOSPHOLIPID HYDRATION STUDIED BY DEUTERON MAGNETIC-RESONANCE SPECTROSCOPY [J].
FINER, EG ;
DARKE, A .
CHEMISTRY AND PHYSICS OF LIPIDS, 1974, 12 (01) :1-16
[8]   A COMMON-SENSE APPROACH TO PEAK PICKING IN 2-DIMENSIONAL, 3-DIMENSIONAL, AND 4-DIMENSIONAL SPECTRA USING AUTOMATIC COMPUTER-ANALYSIS OF CONTOUR DIAGRAMS [J].
GARRETT, DS ;
POWERS, R ;
GRONENBORN, AM ;
CLORE, GM .
JOURNAL OF MAGNETIC RESONANCE, 1991, 95 (01) :214-220
[9]   MEMBRANE DIPOLE POTENTIALS, HYDRATION FORCES, AND THE ORDERING OF WATER AT MEMBRANE SURFACES [J].
GAWRISCH, K ;
RUSTON, D ;
ZIMMERBERG, J ;
PARSEGIAN, VA ;
RAND, RP ;
FULLER, N .
BIOPHYSICAL JOURNAL, 1992, 61 (05) :1213-1223
[10]  
GAWRISCH K, 1978, STUD BIOPHYS, V74, P36