Analysis of glycoconjugate structure/functions requires specialized expertise from various disciplines. Many of these tools and approaches are not only difficult, but also require expensive and complex equipment. We have established our Shared Resource Core to not only contain the components that are most essential for the aims of this PEG, but also that build upon the unique strengths of our participating investigators. Each sub-Core is detailed in their separate sections. Sub-Core 01 - Mass Spectrometry -Drs. van Eyk and Zhang are leaders in mass spectrometric analysis of proteins and glycoproteins. The Core is extraordinarily well equipped. The Core's offerings include: 1) Identification of proteins;2) global quantification of N-linked or O-linked glycoproteins using solidphase extraction of glycopeptides;3) Lectin affinity/MS analyses;4) Monitoring changes in glycosylation by lectin microarrays;5) The use of """"""""Click"""""""" chemistry for analyses of metabolically produced glycoconjugates;6)Glycan profiling by MALDI-MS"""""""" (AXIMA-Resonance) and GlycanAnalyser. 7) Cell surface capture technology for isolation of glycoproteins;2) Targeted capture of soluble glycoproteins from cytoplasm or extracellular environment;3) MRM MS/MS assays for targeted quantification ofglycoproteins and glycosylation sites. Sub-Core C2 - NMR - When possible, glycan structure is best determined by NMR. Dr. Allen Bush is a leading expert in the structural analysis of glycans by NMR. His sub-Core supports the PEG by offering structural expertise for oligosaccharides, polysaccharides, glycopeptides, small glycoproteins and glycolipids. State of the art NMR equipment and methods are available in this sub-Core. Sub-Core C3 - Chemistry - Dr. Kevin Yarema is a leading chemical glycobiologist. His sub-Core will support the PEGs by: 1) providing sugar analogs for """"""""metabolic glycoengineering"""""""" (eg. SCFA-hexosamines); 2) performing custom synthesis of inhibitors (eg. D-PDMP, TMG), azido sugars and sugar nucleotides, glycan-tagging tools and other small molecules. Sub-Core 04 - 0-GlcNAc Resources - Drs. Hart and Zachara are leaders in the analysis of 0-GlcNAc. In support of the PEGs we offer: 1) Tools for detecting 0-GlcNAc, OGT and OGA;2) Develop site-specific 0-GlcNAc antibodies;3) Provide synthetic 0-GlcNAc peptides for antibody production and MS standards;4) Assays for OGT and OGA activity;5) Quantitation of sugar nucleotides &nucleotides;6) Assist with site mapping and quantification on single proteins or globally. This Shared Resource provides key technologies to allow rapid advancement of glycoscience research critical to the mission of the NHLBI.

Public Health Relevance

The Study of the roles of glycoconjugates in disease requires multifaceted approaches. This Shared Resource Core provides state-of-the-art tools, methods and expertise to support not only the study of cardiovascular disease, but also to support the broader goals of the PEGs. Each sub-Core builds upon the unique strengths of our PEG and offers tools and reagents that are not typically available to most researchers.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Program Projects (P01)
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Johns Hopkins University
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Yang, Shuang; Rubin, Abigail; Eshghi, Shadi Toghi et al. (2016) Chemoenzymatic method for glycomics: Isolation, identification, and quantitation. Proteomics 16:241-56
Lam, Maggie P Y; Venkatraman, Vidya; Xing, Yi et al. (2016) Data-Driven Approach To Determine Popular Proteins for Targeted Proteomics Translation of Six Organ Systems. J Proteome Res 15:4126-4134
Fahie, Kamau; Zachara, Natasha E (2016) Molecular Functions of Glycoconjugates in Autophagy. J Mol Biol 428:3305-24
Yang, Weiming; Jackson, Brooks; Zhang, Hui (2016) Identification of glycoproteins associated with HIV latently infected cells using quantitative glycoproteomics. Proteomics 16:1872-80
Hardivillé, Stéphan; Hart, Gerald W (2016) Nutrient regulation of gene expression by O-GlcNAcylation of chromatin. Curr Opin Chem Biol 33:88-94
Miller, William P; Mihailescu, Maria L; Yang, Chen et al. (2016) The Translational Repressor 4E-BP1 Contributes to Diabetes-Induced Visual Dysfunction. Invest Ophthalmol Vis Sci 57:1327-37
Zhu, Yanping; Liu, Ta-Wei; Madden, Zarina et al. (2016) Post-translational O-GlcNAcylation is essential for nuclear pore integrity and maintenance of the pore selectivity filter. J Mol Cell Biol 8:2-16
Hou, Ching-Wen; Mohanan, Vishnu; Zachara, Natasha E et al. (2016) Identification and biological consequences of the O-GlcNAc modification of the human innate immune receptor, Nod2. Glycobiology 26:13-8
Ma, Junfeng; Hart, Gerald W (2016) Mass Spectrometry-Based Quantitative O-GlcNAcomic Analysis. Methods Mol Biol 1410:91-103
Lagerlöf, Olof; Slocomb, Julia E; Hong, Ingie et al. (2016) The nutrient sensor OGT in PVN neurons regulates feeding. Science 351:1293-6

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