Resource for Integrated Glycotechnology
Resource for Integrated Glycotechnology
批准号:
9043132
负责人:
KELLEY W. MOREMEN
金额:
$184.74万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-30 至 2020-01-31
关键词:
AddressAmino SugarsAutomobile DrivingAwarenessBase CompositionBase SequenceBedsBindingBinding ProteinsBiochemicalBiologicalBiological ProcessBiologyCell AdhesionCell LineCell Surface ReceptorsCell surfaceCellsChargeChemicalsChondroitin SulfatesCollaborationsCollectionCommunitiesComplexComputing MethodologiesCoronary heart diseaseDevelopmentDisaccharidesDiseaseEngineeringEpitopesEventExtracellular MatrixFeedbackFertilizationGenerationsGlycobiologyGlycolipidsGlycoproteinsGlycosaminoglycansGoalsGrowthHealthHeparinHeparitin SulfateHeterogeneityHumanImmune System DiseasesIn VitroInflammationLabelLearningLigand BindingLigandsMalariaMalignant NeoplasmsMethodsModelingModificationMolecularNeuromuscular JunctionPathway interactionsPhysiologyPlayPolymersPolysaccharidesProtein-Carbohydrate InteractionProteinsProteoglycanRecombinantsResearch PersonnelResourcesRoleServicesSignal PathwaySignal TransductionSpecificityStructureSugar AcidsSystemTechnologyTestingTrainingUronic AcidsValidationbasecancer cellchemokinecombatdesignepimerizationexperienceextracellularfrontierhuman diseaseinnovationinsightinterdisciplinary approachmacromoleculemorphogensmutantnew technologynovelparasite invasionprotein complexproteoglycan core proteinprototyperesearch and developmentscaffoldsuccesssugarsulfationtechnology developmenttooltraining opportunity
中文摘要
描述(由申请人提供):整合糖技术资源的主要总体目标是开发新颖的集成技术和多学科方法来解决糖生物学中的关键问题。蛋白质-碳水化合物相互作用在细胞表面和细胞外基质的许多生物识别事件中起着至关重要的作用。我们的研究重点是蛋白多糖(pg),其中延伸的,线性的,带电的聚糖聚合物附着在细胞表面或分泌的蛋白质上,这些蛋白质有助于细胞-细胞,细胞-大分子,
英文摘要
DESCRIPTION (provided by applicant): The primary Overall objective of the Resource for Integrated Glycotechnology is to develop novel, integrated technologies and multidisciplinary approaches to solve key problems in glycobiology. Protein-carbohydrate interactions play critical roles in numerous biological recognition events at the cell surface and extracellular matrix. The focus of our studies are proteoglycans (PGs), where extended, linear, charged glycan polymers are attached to cell surface or secreted proteins that contribute to cell-cell, cell-macromolecule,
and cell-matrix interactions and influence numerous biological functions. Studies on protein-PG interactions are a prototype for
more generalized studies on protein-carbohydrate interactions. Despite the critical importance of PGs in diverse biological processes, very little is known about the details of PG interactions with
binding partners or their mechanisms of biological function. As a result, PG-protein interactions are a major technical frontier for contemporary biology. We will address the challenges of PG structures, interactions, and biological functions by leveraging advances in analytical, synthetic,
structural, biochemical and biological tools. Technology Research and Development (TR&D) projects will be applied to the study of several Driving Biomedical Projects (DBPs) that will act as a test beds for the utility of the integrated approaches and provide feedback for new challenges that will spur further technology development. As the technologies mature they will be applied to a collection of Collaborative Projects and use in Analytical Services (C&S) that will
also extend the utility of the technologies to a broader scientific community. Multiple strategies for Dissemination will increase awareness and access to the technology developments and our Training courses (D&T) will provide
direct opportunities for researchers to learn the latest technology developments from Resource staff. The proposal aims to develop technologies (TR&Ds) to advance the goals of the DBPs through ligand identification and validation using PG fragment enrichment approaches, MS-based sequencing and composition analysis, and chemical glycan oligomer synthesis and array generation. Structures of PG-protein complexes will be determined using novel NMR methods and oxidative footprinting approaches and computational methods will predict and validate structure models. Biochemical targets will be generated in large quantities with isotopic labels and further modified to contain paramagnetic tags as needed to facilitate NMR studies. PG core proteins containing engineered glycan polymers will be generated using recombinant expression and cell systems harboring enhanced or mutant PG biosynthetic machinery. Mutant cell lines will also be used to characterize biological functions of PGs in appropriate biological contexts. The combined technology developments will advance our understanding of these critical glycan polymer structures and provide insights into their roles in human physiology and disease.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Economical Modular One-Pot Multienzyme Synthesis of Human Milk Oligosaccharides
-
批准号:10575228
-
项目类别:
-
资助金额:$22.65万
-
财政年份:2023
-
负责人:KELLEY W. MOREMEN
-
依托单位:
2013/2015 Glycobiology Gordon Research Conference & Gordon Research Seminar
-
批准号:8451685
-
项目类别:
-
资助金额:$2.1万
-
财政年份:2013
-
负责人:KELLEY W. MOREMEN
-
依托单位:
QRT-PCR TRANSCRIPT ANALYSIS
-
批准号:8363006
-
项目类别:
-
资助金额:$15.47万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF ERAD- AND UPR-RELATED GENE EXPRESSION
-
批准号:8363017
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
MICROARRAY VALIDATION OF DATA FROM WILD-TYPE AND MGAT5 KNOCK-OUT MOUSE TISSUES
-
批准号:8363111
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
EXPRESSION/LABELING OF GLYCOPROTEINS FOR NMR-BASED STRUCTURE STUDIES
-
批准号:8361783
-
项目类别:
-
资助金额:$17.72万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
N-GLYCAN PROCESSING ENZYMES IN GLYCOPROTEIN MATURATION & QUALITY CONTROL
-
批准号:8361789
-
项目类别:
-
资助金额:$0.18万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF TRANSCRIPTS RELATED TO RAT ASN-LINKED GLYCAN BIOSYNTHESIS
-
批准号:8363015
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
ANALYSIS OF TRANSCRIPTS INVOLVED IN GLYCOCONJUGATE SYNTHESIS IN D MELANOGASTER
-
批准号:8363041
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
CHANGES IN GENE EXPRESSION IN NDST1 & NDST2 KNOCK-OUT MOUSE CELLS
-
批准号:8363110
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
BIOMARKER DISCOVERY FOR PATHOLOGICAL PLACENTAL MALARIA
-
批准号:8363040
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
CHANGES IN GENE EXPRESSION IN EXT1 KNOCK-OUT MOUSE ES CELLS
-
批准号:8363029
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF N-GLYCOSYLATION BY STIMULATION OF THE UNFOLDED PROTEIN RESPONSE
-
批准号:8363016
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
QRT-PCR ANALYSIS OF GENES INVOLVED IN SIALYL-LEWIS X SYNTHESIS
-
批准号:8363112
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF GENE EXPRESSION IN MUCOLIPIDOSIS-II ZEBRAFISH
-
批准号:8363028
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF MUCIN-RELATED GENE EXPRESSION
-
批准号:8363026
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF TRANSCRIPTS INVOLVED IN HUMAN ES CELL DIFFERENTIATION
-
批准号:8363031
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF TRANSCRIPTS INVOLVED IN CORE 1 O-GLYCOSYLATION
-
批准号:8363030
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
REGULATION OF GENE EXPRESSION IN HUMAN BLADDER TISSUE
-
批准号:8363025
-
项目类别:
-
资助金额:$0.34万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
DESIGN & EXPRESSION OF GLYCOSYLTRANSFERASES & GLYCOSIDE HYDROLASES
-
批准号:8361785
-
项目类别:
-
资助金额:$18.42万
-
财政年份:2011
-
负责人:KELLEY W. MOREMEN
-
依托单位:
海外基金