Structural evaluation of phospholipid bicelles for solution-state studies of membrane-associated biomolecules

被引:241
作者
Glover, KJ
Whiles, JA
Wu, GH
Yu, NJ
Deems, R
Struppe, JO
Stark, RE
Komives, EA
Vold, RR
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] City Univ New York Grad Ctr & Coll Staten Isl, Dept Chem, Staten Isl, NY 10314 USA
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90024 USA
关键词
D O I
10.1016/S0006-3495(01)75864-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Several complementary physical techniques have been used to characterize the aggregate structures formed in solutions containing dimyristoylphosphatidylcholine (DMPC)/dihexanoylphosphatidylcholine (DHPC) at ratios of less than or equal to0.5 and to establish their morphology and lipid organization as that of bicelles. P-31 NMR studies showed that the DMPC and DHPC components were highly segregated over a wide range of DMPC/DHPC ratios (q = 0.05-0.5) and temperatures (15 degreesC and 37 degreesC). Only at phospholipid concentrations below 130 mM did the bicelles appear to undergo a change in morphology. These results were corroborated by fluorescence data, which demonstrated the inverse dependence of bicelle size on phospholipid concentration as well as a distinctive change in phospholipid arrangement at low concentrations. In addition, dynamic light scattering and electron microscopy studies supported the hypothesis that the bicellar phospholipid aggregates are disk-shaped. The radius of the planar domain of the disk was found to be directly proportional to the ratio of DMPC/DHPC and inversely proportional to the total phospholipid concentration when the DMPC/DHPC ratio was held constant at 0.5. Taken together, these results suggest that bicelles with low q retain the morphology and bilayer organization typical of their liquid-crystalline counterparts, making them useful membrane mimetics.
引用
收藏
页码:2163 / 2171
页数:9
相关论文
共 40 条
[31]   INFLUENCE OF DILUTION ON THE PHYSICAL STATE OF MODEL BILE SYSTEMS - NMR AND QUASI-ELASTIC LIGHT-SCATTERING INVESTIGATIONS [J].
STARK, RE ;
GOSSELIN, GJ ;
DONOVAN, JM ;
CAREY, MC ;
ROBERTS, MF .
BIOCHEMISTRY, 1985, 24 (20) :5599-5605
[32]   500 MHZ H-1-NMR STUDIES OF BILE-SALT PHOSPHATIDYLCHOLINE MIXED MICELLES AND VESICLES - EVIDENCE FOR DIFFERENTIAL MOTIONAL RESTRAINT ON BILE-SALT AND PHOSPHATIDYLCHOLINE RESONANCES [J].
STARK, RE ;
ROBERTS, MF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 770 (02) :115-121
[33]   Dilute bicellar solutions for structural NMR work [J].
Struppe, J ;
Vold, RR .
JOURNAL OF MAGNETIC RESONANCE, 1998, 135 (02) :541-546
[34]   2H NMR studies of a myristoylated peptide in neutral and acidic phospholipid bicelles [J].
Struppe, J ;
Komives, EA ;
Taylor, SS ;
Vold, RR .
BIOCHEMISTRY, 1998, 37 (44) :15523-15527
[35]   Acidic phospholipid bicelles: A versatile model membrane system [J].
Struppe, J ;
Whiles, JA ;
Vold, RR .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :281-289
[36]   Direct measurement of distances and angles in biomolecules by NMR in a dilute liquid crystalline medium [J].
Tjandra, N ;
Bax, A .
SCIENCE, 1997, 278 (5340) :1111-1114
[37]   Isotropic solutions of phospholipid bicelles: A new membrane mimetic for high-resolution NMR studies of polypeptides [J].
Vold, RR ;
Prosser, RS ;
Deese, AJ .
JOURNAL OF BIOMOLECULAR NMR, 1997, 9 (03) :329-335
[38]   Magnetically oriented phospholipid bilayered micelles for structural studies of polypeptides. Does the ideal bicelle exist? [J].
Vold, RR ;
Prosser, RS .
JOURNAL OF MAGNETIC RESONANCE SERIES B, 1996, 113 (03) :267-271
[39]   Orientation and effects of mastoparan X on phospholipid bicelles [J].
Whiles, JA ;
Brasseur, R ;
Glover, KJ ;
Melacini, G ;
Komives, EA ;
Vold, RR .
BIOPHYSICAL JOURNAL, 2001, 80 (01) :280-293
[40]   SIMULTANEOUS OPTICAL MEASUREMENT OF OSMOTIC AND DIFFUSIONAL WATER PERMEABILITY IN CELLS AND LIPOSOMES [J].
YE, RG ;
VERKMAN, AS .
BIOCHEMISTRY, 1989, 28 (02) :824-829