Department of Chemistry, University of Georgia, 302 East Campus Road, Athens, Georgia 30602, United States.
Anal Chem. 2024 Jan 23;96(3):1185-1194. doi: 10.1021/acs.analchem.3c04290. Epub 2024 Jan 9.
Ion mobility mass spectrometry (IM-MS) is a rapid, gas-phase separation technology that can resolve ions on the basis of their and ratios. Since each class of biomolecule has a unique relationship between size and mass, IM-MS spectra of complex biological samples are organized into trendlines that each contain one type of biomolecule (i.e., lipid, peptide, metabolite). These trendlines can aid in the identification of unknown ions by providing a general classification, while more specific identifications require the conversion of IM arrival times to collision cross section (CCS) values to minimize instrument-to-instrument variability. However, the process of converting IM arrival times to CCS values varies between the different IM devices. Arrival times from traveling wave ion mobility (TWIM) devices must undergo a calibration process to obtain CCS values, which can impart biases if the calibrants are not structurally similar to the analytes. For multiomic mixtures, several different types of calibrants must be used to obtain the most accurate CCS values from TWIM platforms. Here we describe the development of a multiomic CCS calibration tool, MOCCal, to automate the assignment of unknown features to the power law calibration that provides the most accurate CCS value. MOCCal calibrates every experimental arrival time with up to three class-specific calibration curves and uses the difference (in Å) between the calibrated CCS value and CCS vs / regression lines to determine the best calibration curve. Using real and simulated multiomic samples, we demonstrate that MOCCal provides accurately calibrated CCS values for small molecules, lipids, and peptides.
离子淌度质谱(IM-MS)是一种快速的气相分离技术,可根据离子的 和 比来分离离子。由于每种生物分子的大小与质量之间都存在独特的关系,因此复杂生物样品的 IM-MS 谱图会按照每种生物分子(即脂质、肽、代谢物)的趋势线进行组织。这些趋势线可以通过提供一般分类来帮助鉴定未知离子,而更具体的鉴定则需要将 IM 到达时间转换为碰撞截面(CCS)值,以最小化仪器间的可变性。然而,将 IM 到达时间转换为 CCS 值的过程在不同的 IM 设备之间有所不同。行波离子淌度(TWIM)设备的到达时间必须经过校准过程才能获得 CCS 值,如果校准物质与分析物在结构上不相似,这可能会引入偏差。对于多组学混合物,必须使用几种不同类型的校准物质才能从 TWIM 平台获得最准确的 CCS 值。在这里,我们描述了一种多组学 CCS 校准工具 MOCCal 的开发,该工具可自动将未知特征分配给提供最准确 CCS 值的幂律校准。MOCCal 用多达三个特定于类别的校准曲线来校准每个实验到达时间,并使用校准后的 CCS 值与 CCS 与 / 回归线之间的差异(以 Å 为单位)来确定最佳校准曲线。使用真实和模拟的多组学样品,我们证明 MOCCal 可准确地校准小分子、脂质和肽的 CCS 值。