Norwegian Underwater Intervention (NUI), 5848 Bergen, Norway.
Anal Biochem. 2012 Nov 15;430(2):163-70. doi: 10.1016/j.ab.2012.08.019. Epub 2012 Aug 28.
A simple and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based method was developed for the quantification of tetrahydrobiopterin (BH4), dihydrobiopterin (BH2), and biopterin (B) in human umbilical vein endothelial cells (HUVECs). Freshly prepared cell samples were treated with a mixture consisting of 0.2M trichloroacetic acid (TCA) and a cocktail of various antioxidants in order to precipitate proteins and other cellular components and to stabilize red/ox conditions in the lysates. Chromatography of the cell lysates was performed on a Poroshell 120 SB-C18 column (2.7μm, 150×2.1mm) using a stepwise gradient elution made from two mobile phases. Quantification was performed on a triple quadrupole mass spectrometer employing electrospray ionization with the operating conditions as multiple reaction monitoring (MRM) at positive ion mode. Total chromatographic run time was 23min. The method was validated for analysis in HUVECs, and the limits of quantification were 1nM for BH4 and BH2 and 2.5nM for B. Standard curves were linear in the concentration ranges of 1 to 100nM for BH4 and BH2 and 2.5 to 100nM for B. The current study reports a novel method for the simultaneous and direct quantification of BH4, BH2, and B in a single injection.
建立了一种简单、快速的液相色谱-串联质谱(LC-MS/MS)方法,用于定量检测人脐静脉内皮细胞(HUVECs)中的四氢生物蝶呤(BH4)、二氢生物蝶呤(BH2)和生物蝶呤(B)。新鲜制备的细胞样品用包含 0.2M 三氯乙酸(TCA)和各种抗氧化剂混合物处理,以沉淀蛋白质和其他细胞成分,并稳定裂解物中的氧化还原条件。细胞裂解物的色谱在 Poroshell 120 SB-C18 柱(2.7μm,150×2.1mm)上进行,采用两步梯度洗脱,由两种流动相组成。采用电喷雾电离,正离子模式下的多重反应监测(MRM)进行定量分析,三重四极杆质谱仪进行定量分析。总色谱运行时间为 23min。该方法在 HUVECs 中进行了分析验证,BH4 和 BH2 的定量限为 1nM,B 的定量限为 2.5nM。BH4 和 BH2 的标准曲线在 1 至 100nM 浓度范围内呈线性,B 的标准曲线在 2.5 至 100nM 浓度范围内呈线性。本研究报道了一种新的方法,可在单次进样中同时直接定量 BH4、BH2 和 B。