Using Skyline to Analyze Data-Containing Liquid Chromatography, Ion Mobility Spectrometry, and Mass Spectrometry Dimensions

被引:61
作者
MacLean, Brendan X. [1 ]
Pratt, Brian S. [1 ]
Egertson, Jarrett D. [1 ]
MacCoss, Michael J. [1 ]
Smith, Richard D. [2 ]
Baker, Erin S. [2 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[2] Pacific Northwest Natl Lab, Biol Sci Div, 902 Battelle Blvd,MSIN K8-98,POB 999, Richland, WA 99352 USA
关键词
Ion mobility spectrometry; Skyline; Data independent acquisition; Proteomics; DATA-INDEPENDENT ACQUISITION; LABEL-FREE QUANTITATION; PROTEOMICS; IMS; QUANTIFICATION; SEPARATIONS; DISCOVERY; PEPTIDE; SAMPLES;
D O I
10.1007/s13361-018-2028-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in ion mobility spectrometry (IMS) have illustrated its power in determining the structural characteristics of a molecule, especially when coupled with other separations dimensions such as liquid chromatography (LC) and mass spectrometry (MS). However, these three separation techniques together greatly complicate data analyses, making better informatics tools essential for assessing the resulting data. In this manuscript, Skyline was adapted to analyze LC-IMS-CID-MS data from numerous instrument vendor datasets and determine the effect of adding the IMS dimension into the normal LC-MS molecular pipeline. For the initial evaluation, a tryptic digest of bovine serum albumin (BSA) was spiked into a yeast protein digest at seven different concentrations, and Skyline was able to rapidly analyze the MS and CID-MS data for 38 of the BSA peptides. Calibration curves for the precursor and fragment ions were assessed with and without the IMS dimension. In all cases, addition of the IMS dimension removed noise from co-eluting peptides with close m/z values, resulting in calibration curves with greater linearity and lower detection limits. This study presents an important informatics development since to date LC-IMS-CID-MS data from the different instrument vendors is often assessed manually and cannot be analyzed quickly. Because these evaluations require days for the analysis of only a few target molecules in a limited number of samples, it is unfeasible to evaluate hundreds of targets in numerous samples. Thus, this study showcases Skyline's ability to work with the multidimensional LC-IMS-CID-MS data and provide biological and environmental insights rapidly.
引用
收藏
页码:2182 / 2188
页数:7
相关论文
共 29 条
[1]  
[Anonymous], MOL CELL PROTEOMICS
[2]   Simultaneous fragmentation of multiple ions using IMS drift time dependent collision energies [J].
Baker, Erin Shammel ;
Tang, Keqi ;
Danielson, William F., III ;
Prior, David C. ;
Smith, Richard D. .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2008, 19 (03) :411-419
[3]   Enhancing bottom-up and top-down proteomic measurements with ion mobility separations [J].
Baker, Erin Shammel ;
Burnum-Johnson, Kristin E. ;
Ibrahim, Yehia M. ;
Orton, Daniel J. ;
Monroe, Matthew E. ;
Kelly, Ryan T. ;
Moore, Ronald J. ;
Zhang, Xing ;
Theberge, Roger ;
Costello, Catherine E. ;
Smith, Richard D. .
PROTEOMICS, 2015, 15 (16) :2766-2776
[4]   Simultaneous Proteomic Discovery and Targeted Monitoring using Liquid Chromatography, Ion Mobility Spectrometry, and Mass Spectrometry [J].
Burnum-Johnson, Kristin E. ;
Nie, Song ;
Casey, Cameron P. ;
Monroe, Matthew E. ;
Orton, Daniel J. ;
Ibrahim, Yehia M. ;
Gritsenko, Marina A. ;
Clauss, Therese R. W. ;
Shukla, Anil K. ;
Moore, Ronald J. ;
Purvine, Samuel O. ;
Shi, Tujin ;
Qian, Weijun ;
Liu, Tao ;
Baker, Erin S. ;
Smith, Richard D. .
MOLECULAR & CELLULAR PROTEOMICS, 2016, 15 (12) :3694-3705
[5]   Increasing confidence of LC-MS identifications by utilizing ion mobility spectrometry [J].
Crowell, Kevin L. ;
Baker, Erin S. ;
Payne, Samuel H. ;
Ibrahim, Yehia M. ;
Monroe, Matthew E. ;
Slysz, Gordon W. ;
LaMarche, Brian L. ;
Petyuk, Vladislav A. ;
Piehowski, Paul D. ;
Danielson, William F., III ;
Anderson, Gordon A. ;
Smith, Richard D. .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2013, 354 :312-317
[6]   LC-IMS-MS Feature Finder: detecting multidimensional liquid chromatography, ion mobility and mass spectrometry features in complex datasets [J].
Crowell, Kevin L. ;
Slysz, Gordon W. ;
Baker, Erin S. ;
LaMarche, Brian L. ;
Monroe, Matthew E. ;
Ibrahim, Yehia M. ;
Payne, Samuel H. ;
Anderson, Gordon A. ;
Smith, Richard D. .
BIOINFORMATICS, 2013, 29 (21) :2804-2805
[7]   Qualitative and Quantitative Characterization of Plasma Proteins When Incorporating Traveling Wave Ion Mobility into a Liquid Chromatography-Mass Spectrometry Workflow for Biomarker Discovery: Use of Product Ion Quantitation As an Alternative Data Analysis Tool for Label Free Quantitation [J].
Daly, Charlotte E. ;
Ng, Leong L. ;
Hakimi, Amirmansoor ;
Willingale, Richard ;
Jones, Donald J. L. .
ANALYTICAL CHEMISTRY, 2014, 86 (04) :1972-1979
[8]   Label-free quantification in ion mobility-enhanced data-independent acquisition proteomics [J].
Distler, Ute ;
Kuharev, Joerg ;
Navarro, Pedro ;
Tenzer, Stefan .
NATURE PROTOCOLS, 2016, 11 (04) :795-812
[9]  
Distler U, 2014, NAT METHODS, V11, P167, DOI [10.1038/nmeth.2767, 10.1038/NMETH.2767]
[10]   DIA mass spectrometry [J].
Doerr, Allison .
NATURE METHODS, 2015, 12 (01) :35-35