Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry

被引:112
作者
Klein, TR
Kirsch, D
Kaufmann, R
Riesner, D [1 ]
机构
[1] Univ Dusseldorf, Inst Lasermed, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Inst Phys Biol, D-40225 Dusseldorf, Germany
[3] Univ Dusseldorf, Biol Med Forschungszentrum, D-40225 Dusseldorf, Germany
关键词
lipid analysis; MALDI mass spectrometry; membrane localization; prions; sphingolipids;
D O I
10.1515/bchm.1998.379.6.655
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
Sphingolipids were detected in prions, the agents of transmissible spongiform encephalopathies. The analysis was carried out on highly purified, infectious prion rods, which are composed mainly of insoluble aggregates of the N-terminally truncated prion protein, so-called PrP 27-30, Lipid classes were quantified by high performance thin-layer chromatography with a detection limit of 25-50 ng per lipid class. Matrix-assisted laser desorption/ionization mass spectrometry was applied for the first time to lipid analysis in complex biological samples. A newly developed preparation technique improved the sensitivity to 1-20 pg per molecular species, Only the sphingolipids, galactosylceramide and sphingomyelin, were consistently observed in chloroform/methanol (2:1 v/v) extracts of prion rods. The molar ratio of PrP to the sphingolipids was between 2:1 and 40:1, depending on the purity of the prion preparation. The same lipids were also present in the low density fraction of a gradient centrifugation of prion-rods after sonication in 0.2% SDS, From the two alternatives, that the sphingolipids are either required for prion function or are relies from the cellular location of PrP in caveolae, the second alternative appears more plausible since the preparation of highest specific infectivity contained the lowest amount of sphingolipids.
引用
收藏
页码:655 / 666
页数:12
相关论文
共 68 条
  • [1] Prion research: the next frontiers
    Aguzzi, A
    Weissmann, C
    [J]. NATURE, 1997, 389 (6653) : 795 - 798
  • [2] SCRAPIE AGENT - EVIDENCE AGAINST ITS DEPENDENCE FOR REPLICATION ON INTRINSIC NUCLEIC-ACID
    ALPER, T
    HAIG, DA
    CLARKE, MC
    [J]. JOURNAL OF GENERAL VIROLOGY, 1978, 41 (DEC) : 503 - 516
  • [3] SEMIAUTOMATED MULTISAMPLE ANALYSIS OF AMNIOTIC-FLUID LIPIDS BY HIGH-PERFORMANCE THIN-LAYER CHROMATOGRAPHY REFLECTANCE SPECTRODENSITOMETRY
    ALVAREZ, JG
    LUDMIR, J
    [J]. JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1993, 615 (01): : 142 - 147
  • [4] [Anonymous], 1993, CHROMATOGRAPHY ANAL
  • [5] WESTERN-BLOT MAPPING OF DISEASE-SPECIFIC AMYLOID IN VARIOUS ANIMAL SPECIES AND HUMANS WITH TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES USING A HIGH-YIELD PURIFICATION METHOD
    BEEKES, M
    BALDAUF, E
    CASSENS, S
    DIRINGER, H
    KEYES, P
    SCOTT, AC
    WELLS, GAH
    BROWN, P
    GIBBS, CJ
    GAJDUSEK, DC
    [J]. JOURNAL OF GENERAL VIROLOGY, 1995, 76 : 2567 - 2576
  • [6] Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie
    Beekes, M
    Baldauf, E
    Diringer, H
    [J]. JOURNAL OF GENERAL VIROLOGY, 1996, 77 : 1925 - 1934
  • [7] BIOCHEMICAL AND PHYSICAL-PROPERTIES OF THE PRION PROTEIN FROM 2 STRAINS OF THE TRANSMISSIBLE MINK ENCEPHALOPATHY AGENT
    BESSEN, RA
    MARSH, RF
    [J]. JOURNAL OF VIROLOGY, 1992, 66 (04) : 2096 - 2101
  • [8] AN IMPROVED COPPER REAGENT FOR QUANTITATIVE DENSITOMETRIC THIN-LAYER CHROMATOGRAPHY OF LIPIDS
    BITMAN, J
    WOOD, DL
    [J]. JOURNAL OF LIQUID CHROMATOGRAPHY, 1982, 5 (06): : 1155 - 1162
  • [9] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [10] COPURIFICATION OF SP33-37 AND SCRAPIE AGENT FROM HAMSTER BRAIN PRIOR TO DETECTABLE HISTOPATHOLOGY AND CLINICAL-DISEASE
    BOLTON, DC
    RUDELLI, RD
    CURRIE, JR
    BENDHEIM, PE
    [J]. JOURNAL OF GENERAL VIROLOGY, 1991, 72 : 2905 - 2913