化学
亚甲基
衍生化
同位素标记
亚甲蓝
质谱法
氘
碳负离子
氰醇钠
甘氨酸
核苷酸
同位素稀释
动力学同位素效应
色谱法
有机化学
氨基酸
生物化学
物理
催化作用
基因
光催化
量子力学
作者
Li Chen,Gregory S. Ducker,Wenyun Lu,Xin Teng,Joshua D. Rabinowitz
标识
DOI:10.1007/s00216-017-0514-4
摘要
The cofactor tetrahydrofolate (THF) is used to reduce, oxidize, and transfer one-carbon (1C) units required for the synthesis of nucleotides, glycine, and methionine. Measurement of intracellular THF species is complicated by their chemical instability, signal dilution caused by variable polyglutamation, and the potential for interconversion among these species. Here, we describe a method using negative mode liquid chromatography-mass spectrometry (LC-MS) to measure intracellular folate species from mammalian cells. Application of this method with isotope-labeled substrates revealed abiotic interconversion of THF and methylene-THF, which renders their separate quantitation particularly challenging. Chemical reduction of methylene-THF using deuterated sodium cyanoborohydride traps methylene-THF, which is unstable, as deuterated 5-methyl-THF, which is stable. Together with proper sample handling and LC-MS, this enables effective measurements of five active folate pools (THF, 5-methyl-THF, methylene-THF, methenyl-THF/10-formyl-THF, and 5-formyl-THF) representing the biologically important 1C oxidation states of THF in mammalian cells.
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