微尺度高场不对称波形离子迁移谱-质谱法测定碰撞截面

IF 1.8 3区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Kristina Krasnova, Colin S. Creaser, James C. Reynolds
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引用次数: 0

摘要

碰撞截面(CCS)是离子迁移-质谱法(IMS)测量气相离子的重要特征。通常,CCS测量是用漂管IMS或行波IMS进行的。然而。在高场不对称波形离子迁移率(FAIMS)装置中,离子加热效应使CCS测定更具挑战性。本研究探讨利用已知的CCS标准,是否可以用微尺度FAIMS预测CCS。方法采用Owlstone ultraFAIMS微型FAIMS光谱仪与Orbitrap精确质谱联用。使用两种不同的CCS标准混合物(四烷基卤化铵[TAAHs]和聚dl -丙氨酸低聚物)来评估该体系测定CCS的潜力。采用+1、+2电荷态的聚dl -丙氨酸肽进行外标,以测试肽缓激肽醋酸酯和P物质评价CCS对单带电荷和双带电荷肽的测定精度。结果TAAHs和聚dl -丙氨酸均具有良好的相关系数(R2 = 0.99)。在色散场(DF)强度为250 Td时,缓激肽[M + 2H]2+的测定精度与实验值相差±0.5%;该模型对缓激肽[M + H]+的准确性较低(240 Td时为±1.4%)。在250 Td时,P物质的[M + H]+和[M + 2H]2+离子的测定精度分别在±5%和±3%以内,而在较高的DF值下,准确度下降到约5%。结论两种校准剂的CCS与传播性CF之间存在明显的关系。在DF 240-260 Td范围内获得了最佳精度。在较低的DF下,由于溶剂簇加合物对分析物离子的分辨率不足,准确性降低,而在较高的DF值下,透射差成为一个因素。然而,这些数据表明,当被测化合物与所使用的CCS标准具有相似的结构特征时,微尺度FAIMS可以以合理的精度进行CCS测量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Determination of Collisional Cross Section Using Microscale High-Field Asymmetric Waveform ion Mobility Spectroscopy–Mass Spectrometry (FAIMS-MS)

Determination of Collisional Cross Section Using Microscale High-Field Asymmetric Waveform ion Mobility Spectroscopy–Mass Spectrometry (FAIMS-MS)

Rationale

Collisional cross sections (CCS) are an important characteristic of gas-phase ions that are measured using ion mobility-mass spectrometry (IMS). Typically, CCS measurements are performed with drift-tube IMS or travelling-wave IMS. However. in a high-field asymmetric waveform ion mobility (FAIMS) device, ion heating effects make CCS determination more challenging. This research explores whether CCS can be predicted with microscale FAIMS by using known CCS standards.

Methods

An Owlstone ultraFAIMS microscale FAIMS spectrometer was coupled to an Orbitrap Exactive mass spectrometer. Two different CCS standard mixtures (tetraalkylammonium halides [TAAHs] and poly-DL-alanine oligomers) were used to evaluate the system's potential to determine CCS. Test peptide bradykinin acetate and substance P were used to evaluate CCS determination accuracy for singly and doubly charged peptide species using external calibration with a series of poly-DL-alanine peptides for +1, +2 charge states.

Results

Calibrations with excellent correlation coefficients (R2 = 0.99) for both TAAHs and poly-DL-alanine were obtained. Good accuracy of determination was achieved for bradykinin [M + 2H]2+ with a ± 0.5% difference between experimental and published CCS at a dispersion field (DF) strength of 250 Td; the model proved less accurate for bradykinin [M + H]+ (±1.4% at 240 Td). The accuracy of determination for the [M + H]+ and [M + 2H]2+ ions of substance P was within ± 5% and ± 3% at 250 Td, respectively, while at higher DF values, accuracy decreased to approximately 5%.

Conclusions

Distinct relationships were observed between CCS and transmission CF with both calibrants. Optimum accuracy was obtained at DF 240–260 Td. At lower DF, accuracy is reduced by insufficient resolution of analyte ions from solvent cluster adducts, while at higher DF values, poor transmission becomes a factor. Nevertheless, these data suggest microscale FAIMS can conduct CCS measurements with reasonable accuracy when the compound being measured has similar structural features to the CCS standards used.

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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
219
审稿时长
2.6 months
期刊介绍: Rapid Communications in Mass Spectrometry is a journal whose aim is the rapid publication of original research results and ideas on all aspects of the science of gas-phase ions; it covers all the associated scientific disciplines. There is no formal limit on paper length ("rapid" is not synonymous with "brief"), but papers should be of a length that is commensurate with the importance and complexity of the results being reported. Contributions may be theoretical or practical in nature; they may deal with methods, techniques and applications, or with the interpretation of results; they may cover any area in science that depends directly on measurements made upon gaseous ions or that is associated with such measurements.
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