Biological activities of lipopolysaccharides are determined by the shape of their lipid A portion

被引:250
作者
Schromm, AB
Brandenburg, K
Loppnow, H
Moran, AP
Koch, MHJ
Rietschel, ET
Seydel, U
机构
[1] Boston Med Ctr, Maxwell Finland Lab Infect Dis, Boston, MA USA
[2] Res Ctr Borstel, Ctr Med Biosci, Borstel, Germany
[3] Univ Halle Wittenberg, Forschungslab, Halle, Germany
[4] Natl Univ Ireland, Dept Microbiol, Galway, Ireland
[5] European Mol Biol Lab, Hamburg Outstn, Hamburg, Germany
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 07期
关键词
lipid A; molecular shape; agonism; antagonism; X-ray diffraction;
D O I
10.1046/j.1432-1327.2000.01204.x
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
Lipopolysaccharide (LPS) represents a major virulence factor of Gram-negative bacteria ('endotoxin') that can cause septic shock in mammals including man. The lipid anchor of LPS to the outer membrane, lipid A, has a peculiar chemical structure, harbours the 'endotoxic principle' of LPS and is responsible for the expression of pathophysiological effects. Chemically modified lipid A can be endotoxically inactive, but may express strong antagonistic activity against LPS, a property that can be utilized in antisepsis treatment. We show here that these different biological activities are directly correlated with the molecular shape of lipid A. Only (hexaacyl) lipid A with a conical/concave shape, the cross-section of the hydrophobic region being larger than that of the hydrophilic region, exhibited strong interleukin-6 (IL-6)-inducing capacity. Most strikingly, a correlation between a cylindrical molecular shape of lipid A and antagonistic activity was established: IL-6 induction by enterobacterial LPS was inhibited by cylindrically shaped lipid A except for compounds with reduced headgroup charge. The antagonistic action is interpreted by assuming that lipid A molecules intercalate into the cytoplasmic membrane of mononuclear cells, and subsequently blocking of the putative signaling protein by the lipid A with cylindrical shape.
引用
收藏
页码:2008 / 2013
页数:6
相关论文
共 28 条
  • [1] INFLUENCE OF THE SUPRAMOLECULAR STRUCTURE OF FREE LIPID-A ON ITS BIOLOGICAL-ACTIVITY
    BRANDENBURG, K
    MAYER, H
    KOCH, MHJ
    WECKESSER, J
    RIETSCHEL, ET
    SEYDEL, U
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 218 (02): : 555 - 563
  • [2] Characterization of the nonlamellar cubic and HII structures of lipid A from Salmonella enterica serovar Minnesota by X-ray diffraction and freeze-fracture electron microscopy
    Brandenburg, K
    Richter, W
    Koch, MHJ
    Meyer, HW
    Seydel, U
    [J]. CHEMISTRY AND PHYSICS OF LIPIDS, 1998, 91 (01) : 53 - 69
  • [3] E5531, A PURE ENDOTOXIN ANTAGONIST OF HIGH POTENCY
    CHRIST, WJ
    ASANO, O
    ROBIDOUX, ALC
    PEREZ, M
    WANG, YA
    DUBUC, GR
    GAVIN, WE
    HAWKINS, LD
    MCGUINNESS, PD
    MULLARKEY, MA
    LEWIS, MD
    KISHI, Y
    KAWATA, T
    BRISTOL, JR
    ROSE, JR
    ROSSIGNOL, DP
    KOBAYASHI, S
    HISHINUMA, L
    KIMURA, A
    ASAKAWA, N
    KATAYAMA, K
    YAMATSU, I
    [J]. SCIENCE, 1995, 268 (5207) : 80 - 83
  • [4] GOLENBOCK DT, 1991, J BIOL CHEM, V266, P19490
  • [5] STRUCTURAL STUDIES ON THE PHOSPHATE-FREE LIPID-A OF RHODOMICROBIUM-VANNIELII ATCC-17100
    HOLST, O
    BOROWIAK, D
    WECKESSER, J
    MAYER, H
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 137 (1-2): : 325 - 332
  • [6] Purinergic receptor modulation of lipopolysaccharide signaling and inducible nitric-oxide synthase expression in RAW 264.7 macrophages
    Hu, Y
    Fisette, PL
    Denlinger, LC
    Guadarrama, AG
    Sommer, JA
    Proctor, RA
    Bertics, PJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) : 27170 - 27175
  • [7] TOTAL SYNTHESIS OF LIPID-A, ACTIVE PRINCIPLE OF BACTERIAL-ENDOTOXIN
    IMOTO, M
    YOSHIMURA, H
    KUSUMOTO, S
    SHIBA, T
    [J]. PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 1984, 60 (08): : 285 - 288
  • [8] CD11C/CD18, A TRANSMEMBRANE SIGNALING RECEPTOR FOR LIPOPOLYSACCHARIDE
    INGALLS, RR
    GOLENBOCK, DT
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (04) : 1473 - 1479
  • [9] INFLUENCE OF CD14, LBP AND BPI IN THE MONOCYTE RESPONSE TO LPS OF DIFFERENT POLYSACCHARIDE CHAIN-LENGTH
    JAHR, TG
    SUNDAN, A
    LICHENSTEIN, HS
    ESPEVIK, T
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 42 (01) : 119 - 127
  • [10] LINDNER B, 2000, IN PRESS METHODS MOL