ON THE STRUCTURE OF IMMUNE-STIMULATING SAPONIN-LIPID COMPLEXES (ISCOMS)

被引:82
作者
KERSTEN, GFA [1 ]
SPIEKSTRA, A [1 ]
BEUVERY, EC [1 ]
CROMMELIN, DJA [1 ]
机构
[1] STATE UNIV UTRECHT,DEPT PHARMACEUT,UTRECHT,NETHERLANDS
关键词
ISCOM; QUIL-A; SAPONIN; VACCINE;
D O I
10.1016/0005-2736(91)90388-O
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
Immune-stimulating complexes (iscoms) are stable complexes of cholesterol, phospholipid and Quil A, a triterpene saponin mixture in the size range from 40 to 100 nm. They can be used as antigen carriers in subunit vaccines. In this paper it is demonstrated that iscoms are rigid, negatively charged vesicles in which small water soluble molecules like carboxyfluorescein cannot be retained. The negative zeta-potential prevents iscoms from aggregation. The chemical composition of iscoms in one dispersion varied considerably. A typical example of the composition of iscoms is cholesterol/phospholipid/Quil A = 1.0:1.2:6.2 by weight for the iscom matrix, that is iscoms without antigen, and 1.0:1.3:5.1 for antigen-containing iscoms. A hypothetical model for the structure of the iscom matrix and related structures is presented, based on analytical chemical, physico-chemical and electronmicroscopic data. In this model iscoms are considered to be multi-micellar structures, shaped and stabilized by hydrophobic interactions, electrostatic repulsion, steric factors and possibly hydrogen bonds. The individual micelles are relatively flat, ring-shaped structures, the center offering space for one of the two bulky sugar chains of the saponins.
引用
收藏
页码:165 / 171
页数:7
相关论文
共 40 条
[21]   A MOLECULAR-MODEL FOR VESICLE FORMATION [J].
LASIC, DD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 692 (03) :501-502
[22]  
LENTZ BR, 1976, BIOCHEMISTRY-US, V15, P4521, DOI 10.1021/bi00665a029
[23]   CUBIC PHASES AND ISOTROPIC STRUCTURES FORMED BY MEMBRANE-LIPIDS - POSSIBLE BIOLOGICAL RELEVANCE [J].
LINDBLOM, G ;
RILFORS, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 988 (02) :221-256
[24]  
LOVGREN K, 1988, BIOTECHNOL APPL BIOC, V10, P161
[25]   STRUCTURE + ASSEMBLY OF MACROMOLECULAR LIPID COMPLEXES COMPOSED OF GLOBULAR MICELLES [J].
LUCY, JA ;
GLAUERT, AM .
JOURNAL OF MOLECULAR BIOLOGY, 1964, 8 (05) :727-&
[26]   ISCOM, A NOVEL STRUCTURE FOR ANTIGENIC PRESENTATION OF MEMBRANE-PROTEINS FROM ENVELOPED VIRUSES [J].
MOREIN, B ;
SUNDQUIST, B ;
HOGLUND, S ;
DALSGAARD, K ;
OSTERHAUS, A .
NATURE, 1984, 308 (5958) :457-460
[27]   PREVENTION OF EPSTEIN-BARR (EB) VIRUS-INDUCED LYMPHOMA IN COTTONTOP TAMARINS BY VACCINATION WITH THE EB-VIRUS ENVELOPE GLYCOPROTEIN GP340 INCORPORATED INTO IMMUNE-STIMULATING COMPLEXES [J].
MORGAN, AJ ;
FINERTY, S ;
LOVGREN, K ;
SCULLION, FT ;
MOREIN, B .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :2093-2096
[28]  
OSTERHAUS A, 1985, J IMMUNOL, V135, P591
[29]   QUATERNARY STRUCTURE OF THE IMMUNOSTIMULATING COMPLEX (ISCOM) [J].
OZEL, M ;
HOGLUND, S ;
GELDERBLOM, HR ;
MOREIN, B .
JOURNAL OF ULTRASTRUCTURE AND MOLECULAR STRUCTURE RESEARCH, 1989, 102 (03) :240-248
[30]   STRUCTURE OF THE INVERTED HEXAGONAL (HII) PHASE, AND NON-LAMELLAR PHASE-TRANSITIONS OF LIPIDS [J].
SEDDON, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1031 (01) :1-69