FTMS structure elucidation of natural products:: Application to muraymycin antibiotics using ESI multi-CHEF SORI-CID FTMSn, the top-down/bottom-up approach, and HPLC ESI capillary-skimmer CID FTMS

被引:39
作者
McDonald, LA
Barbieri, LR
Carter, GT
Kruppa, G
Feng, XD
Lotvin, JA
Siegel, MM [1 ]
机构
[1] Wyeth Ayerst Res, Chem Sci, Pearl River, NY 10965 USA
[2] Sandia Natl Labs, Livermore, CA 94551 USA
关键词
D O I
10.1021/ac0264731
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The molecular formulas for the structures and substructures of muraymycin antibiotics A1 (C52H90N14O19, MW 1214) and B1 (C49H83N11O18, MW 1113) were determined using electrospray ionization (ESI) Fourier transform mass spectrometry (FTMS). The muraymycin A1 and B1 structures were elucidated by utilizing capillary-skimmer fragmentation with up to five stages of mass spectrometry (MS5). Multi-CHEF, a multiple ion isolation method, was used at each stage of MSn to isolate a parent ion and up to four reference ions, for exact-mass calibration. The parent ions were fragmented by SORI-CID and the product ions internally calibrated with average absolute mass errors less than 1 ppm at each stage in the fragmentation processes. Using the top-down/bottom-up approach, the molecular formulas for the antibiotics were determined by summing the elemental formulas of the neutral losses, obtained by measuring the mass differences (< 500 Da) between the genetically related sequential parent ion masses in the MSn spectra, with the unique elemental formula of the lowest parent ion mass (< 500 Da). The structures of 12 additional compounds in the muraymycin complex were elucidated using HPLC ESI capillary-skimmer CID FTMS by correlating their fragmentation patterns with those of muraymycins A1 and B1. Sequential neutral losses of an aminosugar, a valine, a uridine, and an ester fatty acid from the muraymycin parent ions provided diagnostic fragments for characterization.
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页码:2730 / 2739
页数:10
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