Bilayer properties of totally synthetic C16:0-lactosyl-ceramide

被引:23
作者
Saxena, K
Zimmermann, P
Schmidt, RR
Shipley, GG
机构
[1] Boston Univ, Sch Med, Dept Biophys, Ctr Adv Biomed Res, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Biochem, Ctr Adv Biomed Res, Boston, MA 02118 USA
[3] Univ Konstanz, Fak Chem, D-78457 Constance, Germany
关键词
D O I
10.1016/S0006-3495(00)76593-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Differential scanning calorimetry (DSC) and x-ray diffraction have been used to study the structural and thermal properties of totally synthetic D-erythro-N-palmitoyl-lactosyl-C-18-sphingosine (C16:0-LacCer). Over the temperature range 0-90 degrees C, fully hydrated C16:0-LacCer shows complex thermal transitions characteristic of polymorphic behavior of exclusively bilayer phases. On heating at 5 degrees C/min, hydrated C16:0-LacCer undergoes a complex two-peak endothermic transition with maxima at 69 degrees C and 74 degrees C and a total enthalpy of 14.6 kcal/mol C16:0-LacCer. At a slower heating rate (1.5 degrees C/min), two endothermic transitions are observed at 66 degrees C and 78 degrees C. After cooling to 0 degrees C, the subsequent heating run shows three overlapping endothermic transitions at 66 degrees C, 69 degrees C, and 71.5 degrees C, followed by a chain-melting endothermic transition at 78 degrees C. Two thermal protocols were used to completely convert C16:0-LacCer to its stable, high melting temperature (78 degrees C) form. As revealed by x-ray diffraction, over the temperature range 20-78 degrees C this stable phase exhibits a bilayer structure, periodicity d approximate to 65 Angstrom with an ordered chain packing mode. At the phase transition (78 degrees C) chain melting occurs, and C16:0-LacCer converts to a liquid crystalline bilayer (L-alpha) phase of reduced periodicity d approximate to 59 Angstrom. On cooling from the L-alpha phase, C16:0-LacCer converts to metastable bilayer phases undergoing transitions at 66-72 degrees C. These studies allow comparisons to be made with the behavior of the corresponding C16:0-Cer (Shah et al., 1995. J. Lipid Res. 36:1936-1944) and C16:0-GluCer and C16:0-GalCer (Saxena et al., 1999. J. Lipid Res. 40.839-849). Our systematic studies are aimed at understanding the role of oligosaccharide complexity in regulating glycosphingolipid structure and properties.
引用
收藏
页码:306 / 312
页数:7
相关论文
共 27 条
[1]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[2]   PHASE BEHAVIOR AND STRUCTURAL CHARACTERISTICS OF HYDRATED BOVINE BRAIN GANGLIOSIDES [J].
CURATOLO, W ;
SMALL, DM ;
SHIPLEY, GG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 468 (01) :11-20
[3]   THERMAL-BEHAVIOR OF FRACTIONATED AND UNFRACTIONATED BOVINE BRAIN CEREBROSIDES [J].
CURATOLO, W .
BIOCHEMISTRY, 1982, 21 (08) :1761-1764
[4]   MESSENGER MOLECULES DERIVED FROM MEMBRANE-LIPIDS [J].
EXTON, JH .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (02) :226-229
[5]  
FISHMAN PH, 1993, ADV LIPID RES, V25, P165
[6]   Structure and properties of N-palmitoleoylgalactosylsphingosine (cerebroside) [J].
Haas, NS ;
Shipley, GG .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1995, 1240 (02) :133-141
[7]   FUNCTIONAL-ROLE OF GLYCOSPHINGOLIPIDS IN CELL RECOGNITION AND SIGNALING [J].
HAKOMORI, S ;
IGARASHI, Y .
JOURNAL OF BIOCHEMISTRY, 1995, 118 (06) :1091-1103
[8]  
HANNUN YA, 1994, J BIOL CHEM, V269, P3125
[9]   INHIBITION OF ENTRY OF HIV-1 IN NEURAL CELL-LINES BY ANTIBODIES AGAINST GALACTOSYL CERAMIDE [J].
HAROUSE, JM ;
BHAT, S ;
SPITALNIK, SL ;
LAUGHLIN, M ;
STEFANO, K ;
SILBERBERG, DH ;
GONZALEZSCARANO, F .
SCIENCE, 1991, 253 (5017) :320-323
[10]   STEREOCHEMISTRY AND SIZE OF SUGAR HEAD GROUPS DETERMINE STRUCTURE AND PHASE-BEHAVIOR OF GLYCOLIPID MEMBRANES - DENSITOMETRIC, CALORIMETRIC, AND X-RAY STUDIES [J].
HINZ, HJ ;
KUTTENREICH, H ;
MEYER, R ;
RENNER, M ;
FRUND, R ;
KOYNOVA, R ;
BOYANOV, AI ;
TENCHOV, BG .
BIOCHEMISTRY, 1991, 30 (21) :5125-5138