Unusual Odd-Electron Fragments from Even-Electron Protonated Prodiginine Precursors Using Positive-Ion Electrospray Tandem Mass Spectrometry

被引:48
作者
Chen, Kan [1 ]
Rannulu, Nalaka S. [1 ]
Cai, Yang [1 ,2 ]
Lane, Pat [1 ]
Liebl, Andrea L. [3 ]
Rees, Bernard B. [3 ]
Corre, Christophe [4 ]
Challis, Gregory L. [4 ]
Cole, Richard B. [1 ]
机构
[1] Univ New Orleans, Dept Chem, New Orleans, LA 70148 USA
[2] Childrens Hosp New Orleans, Res Inst Children, New Orleans, LA USA
[3] Univ New Orleans, Dept Biol Sci, New Orleans, LA 70148 USA
[4] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.jasms.2008.08.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Reports of anticancer and immunosuppressive properties have spurred recent interest in the bacterially produced prodiginines. We use electrospray tandem mass spectrometry (ES-MS/MS) io investigate prodigiosin, undecylprodiginine, and streptorubin B (butyl-meta- cycloheptylprodiginine) and to explore their fragmentation pathways to explain the unusual methyl radical loss and consecutive fragment ions that dominate low-energy collision-induced dissociation (CID) mass spectra. The competition between the formation of even-electron ions and radical ions is examined in detail. Theoretical calculations are used to optimize the structures and calculate the energies of both reactants and products using the Gaussian 03 program. Results indicate that protonation occurs on the nitrogen atom that initially held no hydrogen, thus allowing formation of a pseudo-seven-membered ring that constitutes the most stable ground state [M + H](+) structure. From this precursor, experimental data show that methyl radical loss has the lowest apparent threshold but, alternatively, even-electron fragment ions can be formed by loss of a methanol molecule. Computational modeling indicates that methyl radical loss is the more endothermic process in this competition, but the lower apparent threshold associated with methyl radical loss points to a lower kinetic barrier. Additionally, this characteristic and unusual loss of methyl radical (in combination with weaker methanol loss) from each prodiginine is useful for performing constant neutral loss scans to quickly and efficiently identify all prodiginines in a complex biological mixture without any clean-up or purification. The feasibility of this approach has been proven through the identification of a new, low-abundance prodigiosin analog arising from Hahella chejuensis. (J Am Soc Mass Spectrom 2008, 19, 1856-1866) (c) 2008 American Society for Mass Spectrometry
引用
收藏
页码:1856 / 1866
页数:11
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