Department of Molecular Biology, Division of Chemistry and Bioanalytics, University of Salzburg , Hellbrunnerstrasse 34, 5020 Salzburg, Austria.
Anal Chem. 2014 Jan 7;86(1):826-34. doi: 10.1021/ac403390y. Epub 2013 Dec 16.
The characterization of proteins modified with poly(ethylene glycol) (PEG), such as recombinant human granulocyte-colony stimulating factor (PEGylated rhG-CSF or pegfilgrastim), by electrospray ionization-mass spectrometry (ESI-MS) constitutes a challenge due to the overlapping protein charge state pattern and PEG polydispersity. In order to minimize spectral overlaps, charge reduction by means of the addition of amine was applied. Method development for direct-infusion measurements, carried out on an ESI-time-of-flight (ESI-TOF) instrument, demonstrated the potential of triethylamine (TEA) for shifting the charge state pattern toward lower-charged species and of formic acid (FA) for causing higher charging. After successful method transfer to the LTQ Orbitrap XL instrument, isotopically resolved mass spectra could be acquired. With a median mass accuracy of 1.26 ppm, a number-average monoisotopic molecular mass of 40074.64 Da was determined for pegfilgrastim. The direct comparison of three Orbitrap mass spectrometers, namely the LTQ Orbitrap XL, the Exactive, and the Q Exactive, demonstrated that online interfacing to high performance liquid chromatography (HPLC) was only feasible with the Q Exactive, which offers adequate spectral quality on a time scale compatible with chromatographic separation (i.e., 0.2 min acquisition time per chromatographic peak). Finally, the applicability of both direct-infusion Orbitrap MS and HPLC interfaced to Orbitrap MS was demonstrated for the detection of methionine oxidation in pegfilgrastim. Singly, doubly, and triply oxidized species were readily resolved in the chromatogram, while their oxidation status was easily determined from the mass shifts observed in the deconvoluted mass spectra.
由于蛋白质的电荷状态模式和聚乙二醇(PEG)的多分散性重叠,用电喷雾电离 - 质谱(ESI-MS)对与聚乙二醇(PEG)修饰的蛋白质(如重组人粒细胞集落刺激因子(PEGylated rhG-CSF 或 pegfilgrastim))进行特征描述是一个挑战。为了最小化光谱重叠,通过添加胺来进行电荷还原。在 ESI-飞行时间(ESI-TOF)仪器上进行的直接进样测量的方法开发证明了三乙胺(TEA)用于将电荷状态模式转移到低电荷物种的潜力,以及甲酸(FA)用于引起更高电荷的潜力。成功地将方法转移到 LTQ Orbitrap XL 仪器后,可以获得同位素分辨的质谱。在中位质量精度为 1.26 ppm 的情况下,确定 pegfilgrastim 的数均单同位素分子量为 40074.64 Da。三种 Orbitrap 质谱仪(即 LTQ Orbitrap XL、Exactive 和 Q Exactive)的直接比较表明,仅与 Q Exactive 进行在线高效液相色谱(HPLC)接口是可行的,因为 Q Exactive 在与色谱分离兼容的时间尺度上提供了足够的光谱质量(即每个色谱峰的采集时间为 0.2 分钟)。最后,展示了直接进样 Orbitrap MS 和 HPLC 与 Orbitrap MS 接口在 pegfilgrastim 中甲硫氨酸氧化检测中的适用性。在色谱图中,很容易分辨出单、双和三氧化物种,而从解卷积质谱中观察到的质量位移很容易确定它们的氧化状态。