化学
衍生化
质谱法
代谢物
氨基酸
试剂
代谢组学
色谱法
质谱成像
代谢组
碘化物
化学反应
二苯甲酮
代谢途径
反应中间体
化学结构
生物化学
水解
生物分子
串联质谱法
液相色谱-质谱法
鉴定(生物学)
基质(化学分析)
侧链
作者
Tobias Bausbacher,Alessa Henneberg,Stephanie Meyer,S. Schmidt,Aubry K. Miller,Christiane A. Opitz,Carsten Hopf
标识
DOI:10.1002/cmtd.202500090
摘要
Matrix‐assisted laser desorption/ionization mass spectrometry imaging (MALDI‐MSI) is a key spatial omics technology for spatially resolved visualization and direct on‐tissue identification of multiple lipid and metabolite classes. Recently, many on‐tissue chemical derivatization (OTCD) reagents targeting defined functional groups have been introduced to improve sensitivity and/or molecular specificity for compound annotation. Some act as reactive matrices that introduce permanent charges and no longer require (de)protonation for ionization. However, OTCD side reactions are understudied, and it is presently unknown what pseudo metabolites can be generated as OTCD‐derived artifacts. These are compounds that, in principle, exist as bona fide metabolites in tissues but that can also be products of OTCD side reactions. Here, it is demonstrated that besides expected reaction products, the reactive matrix 4‐(anthracen‐9‐yl)‐2‐fluoro‐1‐methylpyridin‐1‐ium iodide (FMP)‐10 can also cause unexpected N ‐ and O ‐lactoylation and even apparent poly‐lactoylation of multiple amino acids through Mukaiyama esterification. Side reactions are unrelated to MALDI laser photochemistry, as they happen in solution and can be readily observed by liquid chromatography–MS/MS. Since N ‐lactoylated amino acids have recently received much attention in sports physiology and obesity research, much care needs to be taken to distinguish true endogenous N ‐lactoylated amino acids from those that are formed by Mukaiyama side reactions.
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