The Institute for Energy Problems of Chemical Physics, Russian Academy of Sciences, Leninskij pr. 38, k.2 Moscow, Russia 119334.
Anal Chem. 2012 Mar 6;84(5):2275-83. doi: 10.1021/ac202804f. Epub 2012 Feb 22.
The fine structure of isotopic peak clusters in mass spectra of reserpine and substance P are measured using Fourier transform ion cyclotron resonance mass spectrometry at a 7 T magnetic field. The resolved peaks in the fine structure consist of (13)C, (15)N, (17)O, (18)O, (2)H, (33)S, (34)S, and combinations of them. A recently introduced high-resolution ion cyclotron resonance cell (Nikolaev, E. N.; Boldin, I. A.; Jertz, R.; Baykut, G. J. Am. Soc. Mass Spectrom. 2011, 22, 1125-1133) is used in these experiments. The positions of the experimentally obtained fine structure peaks on the mass scale agree with the isotopic distribution simulations with ≤200 ppb error. Some deviation from the theoretical isotopic distribution is observed, less abundant peaks in the fine structure patterns are a little suppressed compared to the larger ones. We present a method for atomic composition determination using accurate mass data and fine isotopic structure of the mass spectrum. Our method combines the traditional atomic composition determination from accurate mass data by enumeration of all possible formulas within constraints defined a priori with the estimation of element coefficients from resolved isotopic structures. These estimated values allow one to narrow the search space for the composition and therefore to reduce the number of candidate formulas.
使用傅里叶变换离子回旋共振质谱在 7 T 磁场下测量利血平和 P 物质质谱中同位素峰簇的精细结构。精细结构中分辨出的峰由 (13)C、(15)N、(17)O、(18)O、(2)H、(33)S、(34)S 和它们的组合组成。在这些实验中使用了最近引入的高分辨率离子回旋共振池 (Nikolaev, E. N.; Boldin, I. A.; Jertz, R.; Baykut, G. J. Am. Soc. Mass Spectrom. 2011, 22, 1125-1133)。在质量尺度上,实验获得的精细结构峰的位置与同位素分布模拟的误差在 200 ppb 以内一致。观察到与理论同位素分布的一些偏差,与较大的峰相比,精细结构模式中较少的丰度峰被稍微抑制。我们提出了一种使用精确质量数据和质谱精细同位素结构确定原子组成的方法。我们的方法将传统的原子组成确定方法与从预先定义的约束条件下枚举所有可能公式的精确质量数据相结合,以及从分辨出的同位素结构估计元素系数相结合。这些估计值可以缩小组成的搜索空间,从而减少候选公式的数量。