Standardized workflow for multiplexed charge detection mass spectrometry on orbitrap analyzers

被引:0
作者
Su, Pei [1 ,2 ,3 ,4 ]
Mcgee, John P. [1 ,2 ,3 ,4 ,5 ,6 ]
Hollas, Michael A. R. [6 ]
Fellers, Ryan T. [6 ]
Durbin, Kenneth R. [6 ,7 ]
Greer, Joseph B. [6 ]
Early, Bryan P. [6 ]
Yip, Ping F. [8 ]
Zabrouskov, Vlad [8 ]
Srzentic, Kristina [8 ]
Senko, Michael W. [8 ]
Compton, Philip D. [6 ,9 ]
Kelleher, Neil L. [1 ,2 ,3 ,4 ,6 ,10 ]
Kafader, Jared O. [1 ,2 ,3 ,4 ,6 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[4] Northwestern Univ, Feinberg Sch Med, Evanston, IL 60208 USA
[5] ImmPro Inc, Evanston, IL USA
[6] Northwestern Univ, Chem Life Proc Inst, Prote Ctr Excellence, Evanston, IL 60208 USA
[7] Proteinaceous Inc, Evanston, IL USA
[8] Thermo Fisher Sci, San Jose, CA USA
[9] Integrated Prot Technol, Evanston, IL USA
[10] Northwestern Univ, Feinberg Sch Med, Dept Biochem & Mol Genet, Chicago, IL 60208 USA
基金
美国国家卫生研究院;
关键词
ELECTROSPRAY-IONIZATION; FOURIER-TRANSFORM; TOP-DOWN; PROTEIN COMPLEXES; INDIVIDUAL IONS; HETEROGENEITY; DESORPTION; SENSITIVITY; PROTEOMICS; TRAP;
D O I
10.1038/s41596-024-01091-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Individual ion mass spectrometry (I2MS) is the Orbitrap-based extension of the niche mass spectrometry technique known as charge detection mass spectrometry (CDMS). While traditional CDMS analysis is performed on in-house-built instruments such as the electrostatic linear ion trap, I2MS extends CDMS analysis to Orbitrap analyzers, allowing charge detection analysis to be available to the scientific community at large. I2MS simultaneously measures the mass-to-charge ratios (m/z) and charges (z) of hundreds to thousands of individual ions within one acquisition event, creating a spectral output directly into the mass domain without the need for further spectral deconvolution. A mass distribution or 'profile' can be created for any desired sample regardless of composition or heterogeneity. To assist in reducing I2MS analysis to practice, we developed this workflow for data acquisition and subsequent data analysis, which includes (i) protein sample preparation, (ii) attenuation of ion signals to obtain individual ions, (iii) the creation of a charge-calibration curve from standard proteins with known charge states and finally (iv) producing a meaningful mass spectral output from a complex or unknown sample by using the STORIboard software. This protocol is suitable for users with prior experience in mass spectrometry and bioanalytical chemistry. First, the analysis of protein standards in native and denaturing mode is presented, setting the foundation for the analysis of complex mixtures that are intractable via traditional mass spectrometry techniques. Examples of complex mixtures included here demonstrate the relevant analysis of an intact human monoclonal antibody and its intricate glycosylation patterns.
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页数:34
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