Direct Approach for Qualitative and Quantitative Characterization of Glycoproteins Using Tandem Mass Tags and an LTQ Orbitrap XL Electron Transfer Dissociation Hybrid Mass Spectrometer

被引:42
作者
Ye, Hongping [1 ]
Boyne, Michael T., II [1 ]
Buhse, Lucinda F. [1 ]
Hill, John [2 ]
机构
[1] US FDA, CDER, DPA, St Louis, MO 63101 USA
[2] US FDA, CDER, ONDQA DPAII, Silver Spring, MD 20993 USA
关键词
POSTTRANSLATIONAL MODIFICATIONS; CULTURE-CONDITIONS; PROTEOMIC ANALYSIS; LINKED GLYCANS; CELL-CULTURE; GLYCOSYLATION; PROTEIN; QUANTIFICATION; IDENTIFICATION; ITRAQ;
D O I
10.1021/ac3026465
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The application of multiplexed isobaric tandem mass tag (TMT) labeling and an LTQ Orbitrap XL ETD (electron transfer dissociation) hybrid mass spectrometer as a direct approach for qualitative and quantitative characterization of glycoproteins is reported. Bovine fetuin was used as a model glycoprotein in this study. For online liquid chromatography-mass spectrometry (LC-MS) analysis, high-resolution, mass accurate full scan MS spectra were acquired in the Orbitrap mass analyzer followed by data-dependent tandem mass spectrometry (MS/MS) with alternating collision-induced dissociation (CID), ETD, and higher-energy collisional dissociation (H CD) scans. An additional in-source dissociation scan was used as a highly sensitive and selective detection method for eluting glycosylated peptides. By alternatively using three different dissociation methods, 23 glycoforms from all 5 corresponding glycopeptides were identified from a trypsin digest of bovine fetuin. With ETD, labile glycans were retained without any signs of carbohydrate cleavage with concurrent fragmentation of the peptide backbone. Glycosylation sites were clearly localized from the ETD fragmentation data. Glycan structure elucidation was accomplished using CID. The CID experiments generated fragment ions predominantly from cleavage of glycosidic bonds without breaking the peptide bond. Novel to this method, the TMT labeling protocol was modified and adapted for higher labeling efficiency, and a TriVersa NanoMate was used to reinfuse samples to improve ETD and HCD spectra of glycopeptides. Quantification with TMT was verified based on the HCD spectra from multiple nonglycopeptides and glycopeptides. This method can be used as a qualitative and quantitative technique for direct characterization of glycoproteins and has applicability for detection of counterfeit glycoprotein drug products.
引用
收藏
页码:1531 / 1539
页数:9
相关论文
共 42 条
[1]   Characterization of glycopeptides by combining collision-induced dissociation and electron-transfer dissociation mass spectrometry data [J].
Alley, William R., Jr. ;
Mechref, Yehia ;
Novotny, Milos V. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2009, 23 (01) :161-170
[2]   Robust and sensitive iTRAQ quantification on an LTQ orbitrap mass spectrometer [J].
Bantscheff, Marcus ;
Boesche, Markus ;
Eberhard, Dirk ;
Matthieson, Toby ;
Sweetman, Gavain ;
Kuster, Bernhard .
MOLECULAR & CELLULAR PROTEOMICS, 2008, 7 (09) :1702-1713
[3]   Quantitative mass spectrometry in proteomics: a critical review [J].
Bantscheff, Marcus ;
Schirle, Markus ;
Sweetman, Gavain ;
Rick, Jens ;
Kuster, Bernhard .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 389 (04) :1017-1031
[4]   Appropriate glycosylation of recombinant proteins for human use - Implications of choice of expression system [J].
Brooks, SA .
MOLECULAR BIOTECHNOLOGY, 2004, 28 (03) :241-255
[5]  
Cabrera G, 2005, BIOTECHNOL APPL BIOC, V41, P67
[6]   Identification of protein O-GlcNAcylation sites using electron transfer dissociation mass spectrometry on native peptides [J].
Chalkley, Robert J. ;
Thalhammer, Agnes ;
Schoepfer, Ralf ;
Burlingame, A. L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (22) :8894-8899
[7]  
Chow S.C., 2011, Biosimilars, V1, P13, DOI DOI 10.2147/BS.S20577
[8]   Relative quantification of proteins in human cerebrospinal fluids by MS/MS using 6-plex isobaric tags [J].
Dayon, Loic ;
Hainard, Alexandre ;
Licker, Virginie ;
Turck, Natacha ;
Kuhn, Karsten ;
Hochstrasser, Denis F. ;
Burkhard, Pierre R. ;
Sanchez, Jean-Charles .
ANALYTICAL CHEMISTRY, 2008, 80 (08) :2921-2931
[9]   Targeting glycosylation as a therapeutic approach [J].
Dwek, RA ;
Butters, TD ;
Platt, FM ;
Zitzmann, N .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (01) :65-75
[10]   Safety Issues Specific to Clinical Development of Protein Therapeutics [J].
Haller, C. A. ;
Cosenza, M. E. ;
Sullivan, J. T. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 84 (05) :624-627