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Reviews & Perspectives
4 Results
- Review Special Issue: GlycoproteomicsOpen Access
The Role of Data-Independent Acquisition for Glycoproteomics
Molecular & Cellular ProteomicsVol. 20100042Published online: January 6, 2021- Zilu Ye
- Sergey Y. Vakhrushev
Cited in Scopus: 0In Brief As a highly abundant and diverse post-translational modification, protein glycosylation is challenging to characterize in various approaches including MS. In MS-based proteomics, data-independent acquisition (DIA) has been advanced rapidly and showed outstanding analytical performances. DIA now started to be applied in different facets of glycoproteomics, including deglycosylated and intact N-linked and O-linked glycopeptides, and screening of oxonium ions. We summarized current applications of DIA in glycoproteomics and discussed its limitations and perspectives. - Review Special Issue: GlycoproteomicsOpen Access
Calculating Glycoprotein Similarities From Mass Spectrometric Data
Molecular & Cellular ProteomicsVol. 20100028Published online: January 5, 2021- William E. Hackett
- Joseph Zaia
Cited in Scopus: 0In Brief To understand the roles of glycoproteins in biological processes, it is necessary to quantify the changes that occur to glycosylation at individual sites and to the whole molecule. That glycoprotein glycosylation is inherently heterogeneous means that the distribution of glycoforms at each glycosite must be quantified in order to inform calculation of molecular similarities. We review analytical and statistical methods for determining glycoprotein molecular similarities from glycoproteomics data. - Review Special Issue: GlycoproteomicsOpen Access
Developments in Mass Spectrometry for Glycosaminoglycan Analysis: A Review
Molecular & Cellular ProteomicsVol. 20100025Published online: January 5, 2021- Lauren E. Pepi
- Patience Sanderson
- Morgan Stickney
- I. Jonathan Amster
Cited in Scopus: 0In Brief Glycosaminoglycans (GAGs) participate in a variety of biological functions and have a multitude of medicinal properties. Due to their non template driven biosynthesis, GAGs are produced as nonuniform complex mixtures. Mass spectrometry paired with on-line separation techniques has been utilized to determine the composition of these complex mixtures. Advances in tandem mass spectrometry have also made determining sequence information such as sulfation location and C-5 epimerization possible. This review covers recent developments in the analysis of GAGs using mass spectrometry. - Review Special Issue: GlycoproteomicsOpen Access
A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics
Molecular & Cellular ProteomicsVol. 20100029Published online: December 19, 2020- Nicholas M. Riley
- Carolyn R. Bertozzi
- Sharon J. Pitteri
Cited in Scopus: 0In Brief Interest in mass spectrometry–based glycoproteomics analysis is increasing because of recent advances in instrumentation and data analysis tools. Such studies can provide a wealth of information across a wide spectrum of glycan classes and biological systems. However, many studies require the choice of an enrichment strategy for glycosylated species prior to analysis to obtain the maximum amount of analytical information. Here, common enrichment strategies are reviewed with strengths and weaknesses, and the practical considerations for various methods are discussed.