The RNA Institute, University at Albany, Albany, NY 12222, USA.
J Mass Spectrom. 2013 Jun;48(6):703-12. doi: 10.1002/jms.3207.
The challenges posed by the analysis of mono-nucleotide mixtures by direct infusion electrospray ionization were examined in the context of recent advances of mass spectrometry (MS) technologies. In particular, we evaluated the merits of high-resolution mass analysis, multistep gas-phase dissociation, and ion mobility determinations for the characterization of species with very similar or identical elemental composition. The high resolving power afforded by a linear trap quadrupole-orbitrap allowed the complete differentiation of overlapping isotopic distributions produced by nucleotides that differed by a single mass unit. Resolving (12)C signals from nearly overlapped (13)C contributions provided the exact masses necessary to calculate matching elemental compositions for unambiguous formulae assignment. However, it was the ability to perform sequential steps of gas-phase dissociation (i.e. MS(n)-type analysis) that proved more valuable for discriminating between truly isobaric nucleotides, such as the AMP/dGMP and UMP/ΨMP couples, which were differentiated in the mixture from their unique fragmentation patterns. The identification of diagnostic fragments enabled the deconvolution of dissociation spectra containing the products of coexisting isobars that could not be individually isolated in the mass-selection step. Approaches based on ion mobility spectrometry-MS provided another dimension upon which isobaric nucleotides could be differentiated according to their distinctive mobility behaviors. Subtle structural variations, such as the different positions of an oxygen atom in AMP/dGMP or the glycosidic bond in UMP/ΨMP, produced detectable differences in the respective ion mobility profiles, which enabled the differentiation of the isobaric couples in the mixture. Parallel activation of all ions emerging from the ion mobility element provided an additional dimension for differentiating these analytes on the basis of both mobility and fragmentation properties.
直接进样电喷雾电离分析单核苷酸混合物所带来的挑战,在质谱 (MS) 技术最新进展的背景下进行了考察。特别是,我们评估了高分辨率质量分析、多步气相解离和离子淌度测定在鉴定具有非常相似或相同元素组成的物质方面的优点。线性阱四极杆-Orbitrap 提供的高分辨率允许完全区分单个质量单位差异的核苷酸产生的重叠同位素分布。分辨几乎重叠的 (13)C 贡献的 (12)C 信号提供了计算匹配元素组成的精确质量,以进行明确的公式赋值。然而,能够进行气相解离的连续步骤(即 MS(n)-型分析)对于区分真正等压核苷酸更有价值,例如 AMP/dGMP 和 UMP/ΨMP 对,它们在混合物中从其独特的碎裂模式中得到区分。鉴定诊断片段使能够对包含共存等压物产物的解离光谱进行解卷积,这些产物在质量选择步骤中无法单独分离。基于离子淌度谱-MS 的方法提供了另一个维度,可以根据独特的淌度行为区分等压核苷酸。细微的结构变化,如 AMP/dGMP 中氧原子的不同位置或 UMP/ΨMP 中的糖苷键,在各自的离子淌度谱中产生可检测的差异,从而能够区分混合物中的等压对。从离子淌度元件中同时激活所有离子提供了一个额外的维度,可以根据淌度和碎裂特性对这些分析物进行区分。