Interaction between sulfogalactosylceramide and dimyristoylphosphatidylcholine increases the orientational fluctuation of their lipid hydrocarbon chains

被引:6
作者
Attar, M
Wong, PTT
Kates, M
Carrier, D
Jaklis, P
Tanphaichitr, N [1 ]
机构
[1] Loeb Med Res Inst, Hormone Growth & Dev Res Grp, Ottawa, ON K1Y 4E9, Canada
[2] Ottawa Civic Hosp, Human Invitro Fertilizat Program, Ottawa, ON K1Y 4E9, Canada
[3] Univ Ottawa, Dept Obstet & Gynecol, Ottawa, ON K1H 8M5, Canada
[4] Univ Ottawa, Dept Biochem, Ottawa, ON K1H 8M5, Canada
[5] Univ Ottawa, Dept Microbiol, Ottawa, ON K1H 8M5, Canada
[6] Univ Ottawa, Dept Immunol, Ottawa, ON K1H 8M5, Canada
基金
英国医学研究理事会;
关键词
sulfogalactosylceramide; phosphatidylcholine; liposomes; Fourier-transform infrared spectroscopy; lipid interaction;
D O I
10.1016/S0009-3084(98)00057-7
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 objective of this study was to investigate the interaction between sulfogalactosylceramide (SGC) and dimyristoylphosphatidylcholine (DMPC) in a mixed model liposomal system (molar ratio SGC:DMPC, 2,3). Structural and dynamic changes of the liposome components were monitored by Fourier-transform infrared spectroscopy (FTIR). Thermotropic FTIR analysis of the mixed liposomes showed a single gel/liquid crystalline phase transition, centered at similar to 42 degrees C. Spectral changes of the amide and ester C=O bands arising from functional groups at the interfacial region indicated a reduced hydrogen bonding of these groups in the mixed liposomes. Pressure-tuning FTIR of mixed liposomes showed that the methylene chains of SGC and DMPC were more orientationally disordered than those of the individual lipid SGC liposomes or DMPC liposomes. These results suggest that the mixed liposomes (molar ratio SGC,DMPC, 2:3) consisted of a homogeneous mixture of SGC and DMPC molecules in which mutual shielding reduced hydrogen bonding in the interfacial region, with a concurrent increase in the orientational disorder of the hydrocarbon chains of both SGC and DMPC. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved,
引用
收藏
页码:227 / 238
页数:12
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