Molecular formula analysis by an MS/MS/MS technique to expedite dereplication of natural products

被引:79
|
作者
Konishi, Yasuo
Kiyota, Taira
Draghici, Cristina
Gao, Jin-Ming
Yeboah, Faustinus
Acoca, Stephane
Jarussophon, Suwatchai
Purisima, Enrico
机构
[1] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
[2] NW A & F Univ, Coll Sci, Nat Prod Resource Res Ctr, Yangling 712100, Shaanxi, Peoples R China
[3] Ecopia BioSci Inc, St Laurent, PQ H4S 2A1, Canada
[4] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[5] Natl Sci & Technol Dev Agcy, Natl Nanotechnol Ctr, Bangkok 12120, Thailand
关键词
D O I
10.1021/ac061391o
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A facile and sensitive mass spectrometric method has been developed for the dereplication of natural products. The method provides information about the molecular formula and substructure of a precursor molecule and its fragments, which are invaluable aids in dereplication of natural products at their early stages of purification and characterization. Collision-induced MS/MS technique is used to fragment a precursor ion into several product ions, and individual product ions are selected and subjected to collision-induced MS/MS/MS analysis. This method enables the identification of the fragmentation pathway of a precursor molecule from its first-generation fragments (MS/MS), through to the nth generation product ions (MSn). It also allows for the identification of the corresponding neutral products released (neutral losses). Elements used in the molecular formula analysis include C, H, N, O, and S, as most natural products are constituted by these five elements. High-resolution mass separation and accurate mass measurements afforded the unique identification of molecular formula of small neutral products. Through sequential add-up of the molecular formulas of the small neutral products, the molecular formula of the precursor ion and its productions were uniquely determined. The molecular formula of the precursor molecule was then reversely used to identify or confirm the molecular formula of the neutral products and that of the productions. The molecular formula of the neutral fragments allowed for the identification of substructures, leading to a rapid and efficient characterization of precursor natural product. The method was applied to paclitaxel (C47H51NO14; 853 amu) to identify its molecular formula and its substructures, and to characterize its potential fragmentation pathways. The method was further validated by correctly identifying the molecular formula of minocycline (C23H27N3O7; 457 amu) and piperacillin (C23H27N5O7S; 517 amu).
引用
收藏
页码:1187 / 1197
页数:11
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