Characterization and enrichment of glycoprotein/glycan via multi-functional free radical reagents
Characterization and enrichment of glycoprotein/glycan via multi-functional free radical reagents
批准号:
9441489
负责人:
Jinshan Gao
金额:
$35.66万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-15 至 2022-02-28
关键词:
AddressAmino Acid SequenceBindingBiologicalBiological MarkersCellsChargeChemistryComplexComplex MixturesCouplingDataDetergentsDevelopmentDiabetes MellitusDiagnosticDiscriminationDiseaseDissociationExtracellular MatrixFaceFree RadicalsGenerationsGlycoproteinsGoalsHumanImmune System DiseasesInflammatoryInvestigationLocationMalignant NeoplasmsMass Spectrum AnalysisModificationMolecularMonosaccharidesOutcomePatient MonitoringPeptide Sequence DeterminationPeptidesPharmaceutical PreparationsPhysiologicalPolysaccharidesPropertyProtein AnalysisProtein GlycosylationProtein Sequence AnalysisProteinsRadialReagentReportingResearchResearch ActivityRoleSaltsSamplingSequence AnalysisSignal TransductionSiteSkeletonSolidStructureSurfaceTechniquesTherapeuticbasecancer therapycost effectivedesigndisulfide bondexperiencefrontierglycoprotein structureglycosylationinnovationionizationnovel strategiesprotein profilingpublic health relevanceresponsetool
中文摘要
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英文摘要
Project Summary
Glycoproteins are ubiquitous components of extracellular matrices and cellular surfaces, and have
been reported to have unique structural and functional roles in cell-cell and cell-matrix interactions.
Over 50% of human proteins are estimated to be potentially glycosylated. Alterations of glycan
expression in glycoprotein have been associated with many diseases, such as cancers, diabetes,
and immune disorders. Meanwhile, the identification of glycosylation site is also crucial for
deciphering physiological relevance and potential value as a diagnostic. Therefore characterization
the disease-associated glycoproteins is essential for the understanding of their functions at a
molecular level, and thus benefits the identification of diagnostic glycoprotein and/or glycan
biomarkers and the better design of therapeutic drugs. Over the past decade, mass spectrometry
has become the pivotal technique for glycan and glycoprotein characterization. However, 1) the
structural complexity of glycan moiety, 2) difficulty in determining glycosylation sites, and 3) the low-
abundance of native glycoproteins render the mass spectrometric characterization of glycoprotein
especially challenging. Therefore, efficient enrichment of glycoprotein and/or glycans prior to mass
spectrometry analysis, and facial mass spectrometric analysis of glycoprotein are desirable for the
comprehensive characterization of glycoproteins. Noting that free radicals excel in the
deconstruction of glycan and glycoprotein in a systematic and predictable fashion (preliminary data),
the goal of this research is to develop solid-supported free radical probes (SSFRP) for
glycan moiety enrichment and characterization, and free radial activated glycoprotein
structure elucidation (FRAGPSE) reagent for glycoprotein characterization, especially the
protein sequencing and glycosylation determination. The proposed research activities will bring
an easily accessible tool to simultaneously enrich and characterize glycoproteins, including 1)
enrichment of glycoprotein and glycans from complex mixtures, 2) analysis of protein sequences, 3)
elucidation of glycan moiety structure, and 4) identification of the glycosylation sites. The proposed
research includes (1) design and synthesis of SSFRP and FRAGPSE, (2) examination of the
capability of SSFRP to elucidate glycan structure, (3) examination of the capability of the SSFRP to
enrich and characterize glycans released from glycoproteins, and (4) examination of the capability
of the FRAGPSE to elucidate the structures of glycoproteins. Overall, the successful completion of
proposed approach will result in high-throughput characterization of trace amount of glycoproteins,
allow the characterization of glycoproteins broadly accessible and cost-effective for the end-user.
The proposed research will move the frontier of glycan study forward significantly.
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