Hongo Yayoi, Fukuyama Daisuke, Chen Lee Chuin, Sekimoto Kanako, Watanabe Hiroshi
Okinawa Institute of Science and Technology (OIST), Okinawa, Japan.
Graduate School of Nanobioscience, Yokohama City University, Yokohama, Japan.
J Mass Spectrom. 2025 Jan;60(1):e5102. doi: 10.1002/jms.5102.
LC-ESI-MS/MS is a preferred method for detecting and identifying metabolites, including those that are unpredictable from the genome, especially in basal metazoans like Cnidaria, which diverged earlier than bilaterians and whose metabolism is poorly understood. However, the unexpected appearance of a "ghost peak" for dopamine, which exhibited the same m/z value and MS/MS product ion spectrum during an analysis of Nematostella vectensis, a model cnidarian, complicated its accurate identification. Understanding the mechanism by which "ghost peaks" appear is crucial to accurately identify the monoamine repertoire in early animals so as to avoid misassignments. Verification experiments showed that in-source oxidation of tyramine, which produced an intense signal, was responsible for this "ghost peak." This artifact commonly occurs among aromatic compounds with high signal intensities and appears at the same m/z as their respective in vivo oxidized metabolites. In metabolomics, spectra contain diverse signals from complex biological mixtures, making it difficult to recognize artifact peaks. To prevent misassignments, despite +16 Da differences, adequate chromatographic separation of metabolites from their respective in vivo oxidation precursors is necessary. Whereas both electrolysis and gas-phase corona discharge can cause in-source oxidation in ESI, corona discharge proved to be the dominant factor. Additionally, the presence of multiple oxygen atom sources was suggested by the voltage-dependent mass shift of +16 Da to +18 Da of the "ghost peak" when using O-labeled water as a solvent. Accurate metabolite identification using LC-ESI-MS/MS requires accounting for in-source products that can mimic in vivo products.
液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)是检测和鉴定代谢物的首选方法,包括那些无法从基因组预测的代谢物,尤其是在刺胞动物等基础后生动物中,刺胞动物比两侧对称动物分化更早,其代谢情况了解甚少。然而,在对模式刺胞动物星状海葵进行分析时,多巴胺出现了一个“鬼峰”,该“鬼峰”在分析过程中表现出相同的质荷比(m/z)值和串联质谱(MS/MS)产物离子谱,这使得对其准确鉴定变得复杂。了解“鬼峰”出现的机制对于准确鉴定早期动物中的单胺种类以避免错误归属至关重要。验证实验表明,酪胺的源内氧化产生了强烈信号,这是造成该“鬼峰”的原因。这种假象常见于具有高信号强度的芳香族化合物中,并且出现在与其各自体内氧化代谢物相同的m/z处。在代谢组学中,光谱包含来自复杂生物混合物的各种信号,这使得难以识别假象峰。为防止错误归属,尽管存在+16 Da的差异,但仍需要将代谢物与其各自的体内氧化前体进行充分的色谱分离。虽然电解和气相电晕放电都可在电喷雾电离(ESI)中引起源内氧化,但事实证明电晕放电是主要因素。此外,当使用O标记水作为溶剂时,“鬼峰”的电压依赖性质量位移从+16 Da变为+18 Da,这表明存在多个氧原子源。使用LC-ESI-MS/MS进行准确的代谢物鉴定需要考虑可能模仿体内产物的源内产物。