CHEMISTRY AND BIOLOGY OF HEPARAN SULFATE

硫酸乙酰肝素的化学和生物学

• 批准号: 8516573
• 负责人: Umesh Ramanlal Desai
• 金额: $ 210.25万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-23 至 2018-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8516573
• 关键词: Address; Analytical Chemistry; Animal Welfare; Anticoagulants; Area; Award; Biochemical; Biology; Boxing; Budgets; Businesses; Cell Line; Certification; Chemistry; Cities; Clinical Trials; Code; Country; County; Development; Direct Costs; Disease; Doctor of Philosophy; Economically Deprived Population; Electronic Mail; Embryo; Enzymes; Face; Faculty; Fostering; Future; Glycosaminoglycans; Goals; Hemostatic function; Heparin; Heparin Cofactor II; Heparitin Sulfate; Human Resources; Human Subject Research; In Vitro; Infection; Inflammation; Inflammation Process; Inflammatory; Institutes; Instruction; Knowledge; Laboratories; Last Name; Libraries; Location; Mentors; Methods; Modeling; NIH Program Announcements; Names; Neutrophil Infiltration; Pharmaceutical Chemistry; Phase III Clinical Trials; Polysaccharides; Positioning Attribute; Principal Investigator; Process; Proteins; Province; Recombinant Proteins; Registries; Regulation; Request for Applications; Research; Research Personnel; Resource Development; Resource Sharing; Role; Scientist; Sepsis; Services; Site; Sodium Chloride; Structure; Students; Synthesis Chemistry; Technology; Telefacsimile; Therapeutic Uses; Thrombosis; Time; United States National Institutes of Health; Universities; Utah; Virginia; Woman; Xenograft procedure; abstracting; angiogenesis; chemokine; computational chemistry; computerized tools; cost; design; drug discovery; human embryonic stem cell; in vivo; in vivo Model; inhibitor/antagonist; lung injury; novel; performance site; professor; programs; response; skills; stem; structural biology; tool; xylosides

DESCRIPTION (provided by applicant): This 'The Chemistry and Biology of Heparan Sulfate' proposal is in response to the RFA entitled "Programs of Excellence in Glycosciences (PEG)" (HL-10-026). This PEG consists of four inter-related projects: Project I (Project Leader [PL]: K. Balagurunathan, Univ. of Utah, Salt Lake City, UT) focuses on chemo-enzymatic and 'Click' xyloside-induced synthesis for novel, structurally defined GAGs; Investigating the regulation of HS biosynthetic process and the significance of GAG chain valency; elucidating angiogenesis effects of designed GAGs; and developing inhibitors of HS biosynthetic enzymes to regulate H/HS synthesis in vivo; Project II (PL: U. Desai; Co-Investigators: D. Tollefsen and V. Yadavalli) focuses on elucidating the role of specific and non-specific interactions of H/HS with proteins using computational, biochemical and biophysical technologies; designing specific GAG activators of heparin cofactor II; and developing selected GAGs as clinically useful anticoagulants; Project III (PL: K. Rajarathnam; Co- Investigators: R. Garofalo and J. Iwahara) focuses on understanding the interaction of chemokines with designed H/HS structures using biophysical and structural methods, and developing H/HS structures that modulate neutrophil recruitment process of inflammation occurring in pathological states such as sepsis, lung injury and infection; and Project IV (PL: D. Cooper; Co-Investigators: S. Robson, R. Pierson and A. Azimzadeh) focuses on investigating designed and chemoenzymatically synthesized H/HS agents as anticoagulants in in vitro, ex vivo and in vivo xenotransplantation (xenoTx) models. The central research goals of the PEG utilizes synthetic, computational and analytical chemistry of glycosaminoglycans (GAGs), especially heparin/heparan sulfate (H/HS), to understand their role in modulating hemostasis, thrombosis, inflammation, and angiogenesis, and develop selected agents for use in thrombotic disorders, inflammatory disorders and xenotransplantation. The central skills development goal of the PEG is to mentor three assistant professors, six senior researchers and many other students to be successful glycoscience scientists and mentors. The key resource development goal of this PEG is to develop and make available a library of H/HS structures, computational tools, recombinant proteins, biochemical and biophysical tools and in vitro, ex vivo and in vivo models for GAG studies. This PEG is, thus, a unique, direct and complete effort to discover structurally distinct H/HS for therapeutic use, foster the development of young glycoscience investigators for future faculty positions and establish a shared resource with diverse range of multi-disciplinary glycan research tools. RELEVANCE: This research focuses on synthetic, computational and analytical chemistry of glycosaminoglycans (GAGs), especially heparin/heparan sulfate (H/HS), to understand their role in modulating hemostasis, thrombosis, inflammation, and angiogenesis, and develop selected agents for use in thrombotic and inflammatory disorders, and xenotransplantation. (End of Abstract)

描述（由申请人提供）：这份“硫酸肝素的化学和生物学”提案是对RFA题为“糖苷科学卓越计划（PEG）”（HL-10-026）的回应。该PEG由四个相互关联的项目组成：项目一（项目负责人[PL]: K. Balagurunathan, university of Utah, Salt Lake City， UT）专注于化学酶和“Click”木糖苷诱导合成新型，结构明确的GAGs；探讨HS生物合成过程的调控及GAG链价的意义；阐明设计的GAGs的血管生成作用；开发HS生物合成酶抑制剂，调节体内H/HS合成；项目II （PL: U. Desai；合作研究者：D. Tollefsen和V. Yadavalli）侧重于利用计算、生化和生物物理技术阐明H/HS与蛋白质的特异性和非特异性相互作用的作用；设计特异性GAG型肝素辅助因子II激活剂；并开发选定的gag作为临床有用的抗凝血剂；项目III （PL: K. Rajarathnam，合作研究者：R. Garofalo和J. Iwahara）侧重于利用生物物理和结构方法了解趋化因子与设计的H/HS结构的相互作用，并开发在脓毒症、肺损伤和感染等病理状态下调节炎症中性粒细胞募集过程的H/HS结构；项目IV （PL: D. Cooper；合作研究者：S. Robson， R. Pierson和A. Azimzadeh）专注于研究设计和化学酶合成的H/HS药物在体外，离体和体内异种移植（xenoTx）模型中的抗凝血剂。PEG的中心研究目标是利用糖胺聚糖（GAGs）的合成、计算和分析化学，特别是肝素/硫酸肝素（H/HS），来了解它们在调节止血、血栓形成、炎症和血管生成中的作用，并开发用于血栓性疾病、炎症性疾病和异种移植的选定药物。PEG的核心技能发展目标是指导三名助理教授，六名高级研究员和许多其他学生成为成功的糖科学科学家和导师。该PEG的主要资源开发目标是开发并提供用于GAG研究的H/HS结构库、计算工具、重组蛋白、生化和生物物理工具以及体外、离体和体内模型。因此，这个聚乙二醇是一个独特的，直接的和完整的努力，以发现结构独特的H/HS用于治疗用途，促进年轻糖科学研究者的发展，为未来的教师职位，并建立一个共享资源与各种多学科的糖研究工具。相关：本研究重点研究糖胺聚糖（GAGs）的合成、计算和分析化学，特别是肝素/硫酸肝素（H/HS），以了解它们在调节止血、血栓形成、炎症和血管生成中的作用，并开发用于血栓性和炎症性疾病以及异种移植的药物。（摘要结束）