Detection of free and covalently bound microcystins in animal tissues by liquid chromatography-tandem mass spectrometry

被引:67
作者
Neffling, Milla-Riina [1 ]
Lance, Emilie [2 ]
Meriluoto, Jussi [1 ]
机构
[1] Abo Akad Univ, Dept Biochem & Pharm, FI-20520 Turku, Finland
[2] Univ Rennes 1, CNRS, UMR Ecobio 6553, F-35042 Rennes, France
关键词
Microcystins; MMPB method; Total contamination levels; IN-VIVO EVIDENCE; PROTEIN PHOSPHATASES; LR; LIVER; CYANOBACTERIA; INHIBITOR; NODULARIN; TOXICITY; MUSSELS; BINDING;
D O I
10.1016/j.envpol.2009.10.023
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Microcystins are cyanobacterial hepatotoxins capable of accumulation into animal tissues. The toxins act by inhibiting specific protein phosphatases and both non-covalent and covalent interactions occur. The 2-methyl-3-methoxy-4-phenylbutyric acid (MMPB) method determines the total, i e. the sum of free and protein-bound microcystin in tissues. The aim of the method development in this paper was to tackle the problems with the MMPB methodology. the rather laborious workflow and the loss of material during different steps of the method In the optimised workflow the oxidation recovery was of acceptable level (29-40%), the extraction efficiency good (62-97%), but the signal suppression effect from the matrix remained severe in our system (16-37% signal left) The extraction efficiency for the determination of the free, extractable microcystins, was found to be good, 52-100%, depending on the sample and the toxin variant and concentration (C) 2009 Elsevier Ltd. All rights reserved
引用
收藏
页码:948 / 952
页数:5
相关论文
共 24 条
  • [1] Cyanobacterial toxins: risk management for health protection
    Codd, GA
    Morrison, LF
    Metcalf, JS
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 203 (03) : 264 - 272
  • [2] Mass spectrometric screening method for microcystins in cyanobacteria
    Harada, K
    Murata, H
    Qiang, Z
    Suzuki, M
    Kondo, F
    [J]. TOXICON, 1996, 34 (06) : 701 - 710
  • [3] Inhibition of several protein phosphatases by a non-covalently interacting microcystin and a novel cyanobacterial peptide, nostocyclin
    Hastie, CJ
    Borthwick, EB
    Morrison, LF
    Codd, GA
    Cohen, PTW
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2005, 1726 (02): : 187 - 193
  • [4] HONKANEN RE, 1990, J BIOL CHEM, V265, P19401
  • [5] Proteomics approach on microcystin binding proteins in mouse liver for investigation of microcystin toxicity
    Imanishi, S
    Harada, K
    [J]. TOXICON, 2004, 43 (06) : 651 - 659
  • [6] Mass spectrometric detection of nodularin and desmethylnodularin in mussels and flounders
    Karlsson, K
    Sipiä, V
    Kankaanpää, H
    Meriluoto, J
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 784 (02): : 243 - 253
  • [7] Total microcystin determination using erythro-2-methyl-3-(methoxy-d3)-4-phenylbutyric acid (MMPB-d3) as the internal standard
    Kaya, K
    Sano, T
    [J]. ANALYTICA CHIMICA ACTA, 1999, 386 (1-2) : 107 - 112
  • [8] FORMATION, CHARACTERIZATION, AND TOXICITY OF THE GLUTATHIONE AND CYSTEINE CONJUGATES OF TOXIC HEPTAPEPTIDE MICROCYSTINS
    KONDO, F
    IKAI, Y
    OKA, H
    OKUMURA, M
    ISHIKAWA, N
    HARADA, K
    MATSUURA, K
    MURATA, H
    SUZUKI, M
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (05) : 591 - 596
  • [9] LANCE E, 2009, ENV POLLUT IN PRESS
  • [10] CYANOBACTERIAL MICROCYSTIN-LR IS A POTENT AND SPECIFIC INHIBITOR OF PROTEIN PHOSPHATASE-1 AND PHOSPHATASE-2A FROM BOTH MAMMALS AND HIGHER-PLANTS
    MACKINTOSH, C
    BEATTIE, KA
    KLUMPP, S
    COHEN, P
    CODD, GA
    [J]. FEBS LETTERS, 1990, 264 (02) : 187 - 192