Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Chamblee Campus, Atlanta, GA, 30341, USA.
J Am Soc Mass Spectrom. 2017 Nov;28(11):2319-2329. doi: 10.1007/s13361-017-1756-2. Epub 2017 Aug 11.
We demonstrate the application of in-source nitrogen collision-induced dissociation (CID) that eliminates the need for ester hydrolysis before simultaneous analysis of esterified cholesterol (EC) and triglycerides (TG) along with free cholesterol (FC) from human serum, using normal phase liquid chromatography (LC) coupled to atmospheric pressure chemical ionization (APCI) tandem mass spectrometry (MS/MS). The analysis requires only 50 μL of 1:100 dilute serum with a high-throughput, precipitation/evaporation/extraction protocol in one pot. Known representative mixtures of EC and TG species were used as calibrators with stable isotope labeled analogs as internal standards. The APCI MS source was operated with nitrogen source gas. Reproducible in-source CID was achieved with the use of optimal cone voltage (declustering potential), generating FC, EC, and TG lipid class-specific precursor fragment ions for multiple reaction monitoring (MRM). Using a representative mixture of purified FC, CE, and TG species as calibrators, the method accuracy was assessed with analysis of five inter-laboratory standardization materials, showing -10% bias for Total-C and -3% for Total-TG. Repeated duplicate analysis of a quality control pool showed intra-day and inter-day variation of 5% and 5.8% for FC, 5.2% and 8.5% for Total-C, and 4.1% and 7.7% for Total-TG. The applicability of the method was demonstrated on 32 serum samples and corresponding lipoprotein sub-fractions collected from normolipidemic, hypercholesterolemic, hypertriglyceridemic, and hyperlipidemic donors. The results show that in-source CID coupled with isotope dilution UHPLC-MS/MS is a viable high precision approach for translational research studies where samples are substantially diluted or the amounts of archived samples are limited. Graphical Abstract ᅟ.
我们展示了同源于氮碰撞诱导解离(CID)在源内应用,该方法消除了在使用正相液相色谱(LC)与大气压化学电离(APCI)串联质谱(MS/MS)同时分析人血清中酯化胆固醇(EC)和三酰基甘油(TG)以及游离胆固醇(FC)之前需要进行酯水解的步骤。该分析仅需 50 μL 1:100 稀释血清,采用高通量沉淀/蒸发/提取一锅法。使用 EC 和 TG 种已知代表混合物作为校准物,并使用稳定同位素标记的类似物作为内标。APCI MS 源采用氮气源气体进行操作。通过使用最佳的锥电压(解簇电位),实现了可重现的同源于 CID,从而产生了用于多重反应监测(MRM)的 FC、EC 和 TG 脂质类特异性前体片段离子。使用纯化的 FC、CE 和 TG 种的代表性混合物作为校准物,评估了该方法的准确性,对五种实验室间标准化材料的分析显示总胆固醇(Total-C)的偏差为-10%,总三酰基甘油(Total-TG)的偏差为-3%。对质控池的重复重复分析显示 FC 的日内和日间变异为 5%和 5.8%,总胆固醇(Total-C)的日内和日间变异为 5.2%和 8.5%,总三酰基甘油(Total-TG)的日内和日间变异为 4.1%和 7.7%。该方法应用于从正常脂质、高胆固醇血症、高三酰基甘油血症和高脂血症供体收集的 32 个血清样本和相应的脂蛋白亚组分中。结果表明,同源于 CID 与同位素稀释 UHPLC-MS/MS 相结合,是一种可行的高精度方法,适用于样品大量稀释或存档样品数量有限的转化研究。