Anal Chem. 2019 Feb 5;91(3):2464-2471. doi: 10.1021/acs.analchem.8b05286. Epub 2019 Jan 17.
Coenzyme A (CoA) and acetyl-coenzyme A (acetyl-CoA) are ubiquitous cellular molecules, which mediate hundreds of anabolic and catabolic reactions including energy metabolism. Highly sensitive methods including absorption spectroscopy and mass spectrometry enable their analysis, albeit with many limitations. To date, however, NMR spectroscopy has not been used to analyze these important molecules. Building on our recent efforts, which enabled simultaneous analysis of a large number of metabolites in tissue and blood including many coenzymes and antioxidants ( Anal. Chem. 2016, 88, 4817-24; ibid 2017, 89, 4620-4627), we describe here a new method for identification and quantitation of CoA and acetyl-CoA ex vivo in tissue. Using mouse heart, kidney, liver, brain, and skeletal tissue, we show that a simple H NMR experiment can simultaneously measure these molecules. Identification of the two species involved a comprehensive analysis of the different tissue types using 1D and 2D NMR, in combination with spectral databases for standards, as well as spiking with authentic compounds. Time dependent studies showed that while the acetyl-CoA levels remain unaltered, CoA levels diminish by more than 50% within 24 h, which indicates that CoA is labile in solution; however, degassing the sample with helium gas halted its oxidation. Further, interestingly, we also identified endogenous coenzyme A glutathione disulfide (CoA-S-S-G) in tissue for the first time by NMR and show that CoA, when oxidized in tissue extract, also forms the same disulfide metabolite. The ability to simultaneously visualize absolute concentrations of CoA, acetyl-CoA, and endogenous CoA-S-S-G along with redox coenzymes (NAD, NADH, NADP, NADPH), energy coenzymes (ATP, ADP, AMP), antioxidants (GSH, GSSG), and a vast pool of other metabolites using a single 1D NMR spectrum offers a new avenue in the metabolomics field for investigation of cellular function in health and disease.
辅酶 A(CoA)和乙酰辅酶 A(acetyl-CoA)是普遍存在于细胞内的分子,介导包括能量代谢在内的数百种合成和分解反应。尽管存在许多局限性,但包括吸收光谱和质谱在内的高度敏感方法可以对其进行分析。然而,迄今为止,NMR 光谱尚未用于分析这些重要分子。基于我们最近的努力,我们能够同时分析组织和血液中的大量代谢物,包括许多辅酶和抗氧化剂(分析化学。2016 年,88,4817-24;同上 2017 年,89,4620-4627),我们在这里描述了一种新的方法,用于在组织中对 CoA 和乙酰 CoA 进行体外鉴定和定量。使用小鼠心脏、肾脏、肝脏、大脑和骨骼组织,我们表明,一个简单的 H NMR 实验可以同时测量这些分子。两种物质的鉴定涉及使用 1D 和 2D NMR 对不同组织类型进行全面分析,结合标准的光谱数据库以及用真实化合物进行加标。时程研究表明,虽然乙酰 CoA 水平保持不变,但 CoA 水平在 24 小时内减少了 50%以上,这表明 CoA 在溶液中不稳定;然而,用氦气对样品进行脱气可阻止其氧化。此外,有趣的是,我们还首次通过 NMR 在组织中鉴定出内源性辅酶 A 谷胱甘肽二硫化物(CoA-S-S-G),并表明 CoA 在组织提取物中氧化时也形成相同的二硫化物代谢物。使用单个 1D NMR 谱同时可视化 CoA、乙酰 CoA 和内源性 CoA-S-S-G 的绝对浓度以及氧化还原辅酶(NAD、NADH、NADP、NADPH)、能量辅酶(ATP、ADP、AMP)、抗氧化剂(GSH、GSSG)和其他大量代谢物的能力为代谢组学领域提供了一个新的途径,用于研究健康和疾病状态下的细胞功能。