Nano liquid chromatography with hybrid quadrupole time-of-flight mass spectrometry for the determination of yessotoxin in marine phytoplankton

被引:14
作者
Cañás, IR [1 ]
Hamilton, B [1 ]
Amandi, MF [1 ]
Furey, A [1 ]
James, KJ [1 ]
机构
[1] Cork Inst Technol, Dept Chem, Mass Spectrometry Ctr Proteom & Biotoxin res, PROTEOBIO, Cork, Ireland
关键词
yessotoxin; phytoplankton;
D O I
10.1016/j.chroma.2004.07.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Studies of yessotoxin involving confirmation of fragmentation processes using a high-resolution orthogonal hybrid quadrupole time-of-flight (QqTOF) mass spectrometer and nanoLC hybrid quadrupole TOF MS have been undertaken. The fragmentation of YTX was studied in negative mode using nano electrospray (nanoESI) QqTOF mass spectrometry. Three major molecule-related ions were observed, [M - 2Na + H](-), [M - Na](-) and [M - 2Na](2-), and fragmentation of the latter was studied in detail. This showed that product ions were formed as a consequence of charge-remote fragmentation processes that included a strong directional cleavage of the polyether rings of YTX. NanoLC coupled with QqTOF MS was used to determine YTX in small samples of the phytoplankton, Protoceratium reticulatum, by monitoring the [M - 2Na](2-) ion at m/z 570. A PepMap C-18 nanoLC column (75 mum x 10 cm, 100 A, 3 mum, LC Packings) was used and the solvent was acetonitrile/water (90:10 (v/v)) containing 1 mM ammonium acetate, at a flow rate of 400 nl/min, for 30 min. Calibrations obtained with YTX standard solutions were linear over four orders of magnitude, 0.75-250 ng/ml; r(2) = 0.9947-0.9998. Phytoplankton cells (ca. 100-300) were picked, extracted with methanol/water (40:60), and the YTX concentration was determined over the range 0.011-0.020 ng/cell. The detection limit (3 x S/N) of this method was ca. 0.5 pg YTX on-column. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 256
页数:4
相关论文
共 15 条
[1]   Liquid chromatography with electrospray ion-trap mass spectrometry for the determination of yessotoxins in shellfish [J].
Amandi, MF ;
Furey, A ;
Lehane, M ;
Ramstad, H ;
James, KJ .
JOURNAL OF CHROMATOGRAPHY A, 2002, 976 (1-2) :329-334
[2]   Direct detection of yessotoxin and its analogues by liquid chromatography coupled with electrospray ion trap mass spectrometry [J].
Ciminiello, P ;
Dell'Aversano, C ;
Fattorusso, E ;
Forino, M ;
Magno, S ;
Poletti, R .
JOURNAL OF CHROMATOGRAPHY A, 2002, 968 (1-2) :61-69
[3]   New approach to the direct detection of known and new diarrhoeic shellfish toxins in mussels and phytoplankton by liquid chromatography-mass spectrometry [J].
Draisci, R ;
Palleschi, L ;
Giannetti, L ;
Lucentini, L ;
James, KJ ;
Bishop, AG ;
Satake, M ;
Yasumoto, T .
JOURNAL OF CHROMATOGRAPHY A, 1999, 847 (1-2) :213-221
[4]  
Draisci R, 1998, RAPID COMMUN MASS SP, V12, P1291, DOI 10.1002/(SICI)1097-0231(19981015)12:19<1291::AID-RCM314>3.0.CO
[5]  
2-Y
[6]   Quantitative determination of marine toxins associated with diarrhetic shellfish poisoning by liquid chromatography coupled with mass spectrometry [J].
Goto, H ;
Igarashi, T ;
Yamamoto, M ;
Yasuda, M ;
Sekiguchi, R ;
Watai, M ;
Tanno, K ;
Yasumoto, T .
JOURNAL OF CHROMATOGRAPHY A, 2001, 907 (1-2) :181-189
[7]   Liquid chromatography with fluorimetric, mass spectrometric and tandem mass spectrometric detection for the investigation of the seafood-toxin-producing phytoplankton, Dinophysis acuta [J].
James, KJ ;
Bishop, AG ;
Gillman, M ;
Kelly, SS ;
Roden, C ;
Draisci, R ;
Lucentini, L ;
Giannetti, L ;
Boria, P .
JOURNAL OF CHROMATOGRAPHY A, 1997, 777 (01) :213-221
[8]   ISOLATION AND STRUCTURE OF YESSOTOXIN, A NOVEL POLYETHER COMPOUND IMPLICATED IN DIARRHETIC SHELLFISH POISONING [J].
MURATA, M ;
KUMAGAI, M ;
LEE, JS ;
YASUMOTO, T .
TETRAHEDRON LETTERS, 1987, 28 (47) :5869-5872
[9]   NEGATIVE-ION FAST-ATOM-BOMBARDMENT TANDEM MASS-SPECTROMETRY FOR THE STRUCTURAL STUDY OF POLYETHER COMPOUNDS - STRUCTURAL VERIFICATION OF YESSOTOXIN [J].
NAOKI, H ;
MURATA, M ;
YASUMOTO, T .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1993, 7 (03) :179-182
[10]  
Quilliam M. A., 1996, APPL LC MS ENV CHEM, P415, DOI DOI 10.1037//0003-066X.46.5.506