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High-Throughput Glycomics and Glycoproteomics

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Cover of 'High-Throughput Glycomics and Glycoproteomics'

Table of Contents

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    Book Overview
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    Chapter 1 Ubiquitous Importance of Protein Glycosylation.
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    Chapter 2 Laboratory Experimental Design for a Glycomic Study.
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    Chapter 3 High-Throughput Analysis of the IgG N-Glycome by UPLC-FLR.
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    Chapter 4 High-Throughput Analysis of IgG Fc Glycopeptides by LC-MS.
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    Chapter 5 Sialic Acid Derivatization for the Rapid Subclass- and Sialic Acid Linkage-Specific MALDI-TOF-MS Analysis of IgG Fc-Glycopeptides.
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    Chapter 6 The Use of Multiple Reaction Monitoring on QQQ-MS for the Analysis of Protein- and Site-Specific Glycosylation Patterns in Serum.
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    Chapter 7 Analysis of Permethylated Glycan by Liquid Chromatography (LC) and Mass Spectrometry (MS).
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    Chapter 8 High-Throughput Analysis of the Plasma N-Glycome by UHPLC.
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    Chapter 9 Site-Specific N- and O-Glycopeptide Analysis Using an Integrated C18-PGC-LC-ESI-QTOF-MS/MS Approach.
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    Chapter 10 Analysis of Milk Oligosaccharides by Mass Spectrometry.
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    Chapter 11 N- and O-Glycomics from Minor Amounts of Formalin-Fixed, Paraffin-Embedded Tissue Samples.
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    Chapter 12 Carbohydrate Microarray Technology Applied to High-Throughput Mapping of Plant Cell Wall Glycans Using Comprehensive Microarray Polymer Profiling (CoMPP).
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    Chapter 13 Analysis of Invertebrate and Protist N-Glycans.
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    Chapter 14 High-Throughput and High-Sensitivity Mass Spectrometry-Based N-Glycomics of Mammalian Cells.
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    Chapter 15 Analysis of N-Glycosylation of Total Membrane Proteins.
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    Chapter 16 HILIC-UPLC Analysis of Brain Tissue N-Glycans.
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    Chapter 17 Automated Integration of a UPLC Glycomic Profile.
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    Chapter 18 Databases and Associated Tools for Glycomics and Glycoproteomics.
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    Chapter 19 High-Throughput N-Glycan Analysis with Rapid Magnetic Bead-Based Sample Preparation.
Attention for Chapter 5: Sialic Acid Derivatization for the Rapid Subclass- and Sialic Acid Linkage-Specific MALDI-TOF-MS Analysis of IgG Fc-Glycopeptides.
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Chapter title
Sialic Acid Derivatization for the Rapid Subclass- and Sialic Acid Linkage-Specific MALDI-TOF-MS Analysis of IgG Fc-Glycopeptides.
Chapter number 5
Book title
High-Throughput Glycomics and Glycoproteomics
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6493-2_5
Pubmed ID
Book ISBNs
978-1-4939-6491-8, 978-1-4939-6493-2
Authors

Noortje de Haan, Karli R. Reiding, Manfred Wuhrer

Editors

Gordan Lauc, Manfred Wuhrer

Abstract

Matrix-assisted laser desorption/ionization (MALDI)-time-of-flight (TOF)-mass spectrometry (MS) is a highly suitable method for the rapid analysis of IgG glycopeptides, providing a wealth of structural information. A limitation of this approach is that it generates a bias when analyzing sialylated species due to the labile nature of sialic acid glycosidic linkages. One way to overcome this problem is by chemical derivatization of the sialic acids. The method presented here results in both the stabilization of the sialic acids, as well as the differentiation of α2,3- and α2,6-linked sialic acids by mass. Described in this chapter are the isolation of IgG from plasma or serum, tryptic digestion of the samples, derivatization, and finally MALDI-TOF-MS measurement and data analysis.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 38%
Lecturer 2 25%
Student > Master 1 13%
Unknown 2 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 38%
Veterinary Science and Veterinary Medicine 1 13%
Agricultural and Biological Sciences 1 13%
Unknown 3 38%