The dual role of lipopolysaccharide as effector and target molecule

被引:40
作者
Wiese, A [1 ]
Brandenburg, K [1 ]
Ulmer, AJ [1 ]
Seydel, U [1 ]
Müller-Loennies, S [1 ]
机构
[1] Res Ctr Borstel, Ctr Med & Biosci, D-23845 Borstel, Germany
关键词
complement activation; endotoxicity; lipopolysaccharide; lipopolysaccharide receptors; outer membrane; porins;
D O I
10.1515/BC.1999.097
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
Lipopolysaccharides (LPS) are major integral components of the outer membrane of Gram-negative bacteria being exclusively located in its outer leaflet facing the bacterial environment. Chemically they consist in different bacterial strains of a highly variable O-specific chain, a less variable core oligosaccharide, and a lipid component, termed lipid A, with low structural variability, LPS participate in the physiological membrane functions and are, therefore, essential for bacterial growth and viability. They contribute to the low membrane permeability and increase the resistance towards hydrophobic agents. They are also the primary target for the attack of antibacterial drugs and proteins such as components of the host's immune response. When set free LPS elicit, in higher organisms, a broad spectrum of biological activities. They play an important role in the manifestation of Gram-negative infection and are therefore termed endotoxins. Physico-chemical parameters such as the molecular conformation and the charges of the lipid A portion, which is responsible for endotoxin-typical biological activities and is therefore termed the 'endotoxic principle' of LPS, are correlated with the biological activity of chemically different LPS.
引用
收藏
页码:767 / 784
页数:18
相关论文
共 181 条
[1]  
[Anonymous], 1987, Escherichia coli and Salmonella typhimurium: cellular and molecular biology
[2]  
ANTONOV VF, 1976, STUD BIOPHYS, V58, P87
[3]   Critical aggregation concentrations of gram-negative bacterial lipopolysaccharides (LPS) [J].
Aurell, CA ;
Wistrom, AO .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 253 (01) :119-123
[4]   RESISTANCE CHANGES IN LIPID BILAYERS - IMMUNOLOGICAL APPLICATIONS [J].
BARFORT, P ;
ARQUILLA, ER ;
VOGELHUT, PO .
SCIENCE, 1968, 160 (3832) :1119-+
[5]   Crystal structure of human BPI and two bound phospholipids at 2.4 angstrom resolution [J].
Beamer, LJ ;
Carroll, SF ;
Eisenberg, D .
SCIENCE, 1997, 276 (5320) :1861-1864
[6]   INHIBITION OF LIPOPOLYSACCHARIDE BIOSYNTHESIS AND CELL-GROWTH FOLLOWING INACTIVATION OF THE KDTA GENE IN ESCHERICHIA-COLI [J].
BELUNIS, CJ ;
CLEMENTZ, T ;
CARTY, SM ;
RAETZ, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27646-27652
[7]   SINGLE-CHANNEL ANALYSIS OF THE CONDUCTANCE FLUCTUATIONS INDUCED IN LIPID BILAYER-MEMBRANES BY COMPLEMENT PROTEINS C5B-9 [J].
BENZ, R ;
SCHMID, A ;
WIEDMER, T ;
SIMS, PJ .
JOURNAL OF MEMBRANE BIOLOGY, 1986, 94 (01) :37-45
[8]   PERMEATION OF HYDROPHILIC MOLECULES THROUGH THE OUTER-MEMBRANE OF GRAM-NEGATIVE BACTERIA - REVIEW ON BACTERIAL PORINS [J].
BENZ, R ;
BAUER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 176 (01) :1-19
[9]  
BERRIER C, 1993, J MEMBRANE BIOL, V133, P119
[10]   INTERACTION OF POLYMYXIN-B1 AND POLYMYXIN-B1 NONAPEPTIDE WITH PHOSPHATIDIC-ACID MONOLAYER AND BILAYER-MEMBRANES [J].
BEURER, G ;
WARNCKE, F ;
GALLA, HJ .
CHEMISTRY AND PHYSICS OF LIPIDS, 1988, 47 (02) :155-163