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采用质谱策略结合平行反应监测和多重反应监测对 C-谷氨酰胺同位素示踪实验中的 C 标记非必需氨基酸进行表征和定量。

Characterization and Determination of C-Labeled Nonessential Amino Acids in a C-Glutamine Isotope Tracer Experiment with a Mass Spectrometry Strategy Combining Parallel Reaction Monitoring and Multiple Reaction Monitoring.

机构信息

State Key Laboratory of Environmental and Biological Analysis, Department of Chemistry, Hong Kong Baptist University, Hong Kong 999077, China.

Ministry of Education Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.

出版信息

Anal Chem. 2021 Oct 12;93(40):13564-13571. doi: 10.1021/acs.analchem.1c02554. Epub 2021 Sep 27.

Abstract

Isotopic tracer, a powerful technique for metabolic pathway analysis, is currently widely applied in metabolic flux analysis. However, the qualitative and quantitative analyses of C-labeled metabolites pose great challenges, especially in complex biological sample matrices. Here, we present an integrated method for the qualitative and quantitative analyses of various isotopologues and isotopomers of C-labeled nonessential amino acids (NEAAs) in HepG2 cells incubated with C-glutamine (Gln) based on ultra-high-performance liquid chromatography (UHPLC) coupled with tandem mass spectrometry (MS). First, accurate mass-to-charge (/) values of protonated isotopologues and elution time of standards were simultaneously analyzed to characterize C-labeled NEAAs by high-resolution Orbitrap MS in the parallel reaction monitoring (PRM) mode. Second, isotopologues and isotopomers of C-labeled NEAAs were investigated in HepG2 cells incubated with C-Gln at different time points. Ultimately, a total of 66 multiple reaction monitoring (MRM) transitions were performed by UHPLC coupled with triple quadrupole MS. Among them, 29 MRM transitions were monitored for pure metabolites (unambiguously identified). The other 37 MRM transitions were monitored for mixtures with exactly identical MRM transitions and retention time. The application of targeted profiling of C-labeled NEAAs in the dynamic C-labeling experiment indicated that the concentration-time profiles of NEAAs were different from each other. The concentrations of most C-labeled Gln, Glu, Pro, and Asp altered after C-Gln incubation, indicating that Gln plays a fundamental role in the biosynthesis of Glu, Pro, and Asp. The proposed PRM-MRM combination mode LC-MS approach is expected to provide valuable insights into analyses of isotope-labeled metabolites in isotope tracer experiments.

摘要

稳定同位素示踪剂是一种用于代谢途径分析的强大技术,目前广泛应用于代谢通量分析中。然而,C 标记代谢物的定性和定量分析具有很大的挑战性,特别是在复杂的生物样本基质中。在这里,我们提出了一种基于超高效液相色谱(UHPLC)与串联质谱(MS)联用的方法,用于定性和定量分析用 C-谷氨酰胺(Gln)孵育的 HepG2 细胞中各种 C 标记的非必需氨基酸(NEAAs)的同位素异构体和同量异位体。首先,通过高分辨率轨道阱 MS 在平行反应监测(PRM)模式下同时分析质子化同位素异构体的精确质量电荷(/)值和标准品的洗脱时间,以表征 C 标记的 NEAAs。其次,研究了在不同时间点用 C-Gln 孵育的 HepG2 细胞中 C 标记的 NEAAs 的同位素异构体和同量异位体。最终,通过 UHPLC 与三重四极杆 MS 共进行了 66 个多重反应监测(MRM)转换。其中,29 个 MRM 转换用于监测纯代谢物(明确鉴定)。其他 37 个 MRM 转换用于监测具有完全相同的 MRM 转换和保留时间的混合物。C 标记的 NEAAs 靶向分析在动态 C 标记实验中的应用表明,NEAAs 的浓度-时间曲线彼此不同。大多数 C 标记的 Gln、Glu、Pro 和 Asp 的浓度在 C-Gln 孵育后发生变化,表明 Gln 在 Glu、Pro 和 Asp 的生物合成中起着基本作用。所提出的 PRM-MRM 组合模式 LC-MS 方法有望为同位素示踪实验中同位素标记代谢物的分析提供有价值的见解。

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