STRUCTURE DETERMINATION OF TRANSMEMBRANE CARBOHYDRATE TRANSPORTER PROTEINS

跨膜碳水化合物转运蛋白的结构测定

• 批准号: 8361721
• 负责人: Jun-Yong Choe
• 金额: $ 0.55万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-04-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8361721
• 关键词: Affect; Carbohydrates; Carrier Proteins; Cell membrane; Cells; Diabetes Mellitus; Diagnostic Imaging; Drug or chemical Tissue Distribution; Energy-Generating Resources; Fructose; Funding; GLUT2 gene; Glucose; Glucose Transporter; Goals; Grant; Homologous Gene; Human; Life; Ligands; Malignant Neoplasms; National Center for Research Resources; Principal Investigator; Protein translocation; Research; Research Infrastructure; Resources; SLC2A1 gene; Source; Structure; Substrate Specificity; System; United States National Institutes of Health; base; cost; structural biology; three dimensional structure

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. The goal of this project is to determine the structural basis of glucose transporters (GLUTs or SLC2) function. GLUTs are transmembrane proteins that transport carbohydrates (glucose, fructose and others), major energy sources for living cells, across cell membranes. Fourteen human GLUTs indentified so far share similar sequences, but have different substrate specificity and tissue distribution. The activity or/and localization of GLUT2, 4 and 5 are affected in diabetes. Ligands of GLUTs are used in diagnostic imaging of cancers and are emerging as new alternatives in the treatment of human cancers. Despite the overriding importance of GLUTs, there is no three dimensional structure information available for any of the human glucose transporters or for their homologues. Determining the 3D structure of any GLUT will be a remarkable breakthrough in the study of this fundamental transport system and will open new research avenues.

这个子项目是利用资源的许多研究子项目之一。 由NIH/NCRR资助的中心拨款提供。对子项目的主要支持 子项目的首席调查员可能是由其他来源提供的， 包括美国国立卫生研究院的其他来源。为子项目列出的总成本可能 表示该子项目使用的中心基础设施的估计数量， 不是由NCRR赠款提供给次级项目或次级项目工作人员的直接资金。 该项目的目标是确定葡萄糖转运蛋白(Gluts或SLC2)功能的结构基础。谷氨酸是一种跨膜蛋白，可以跨细胞膜运输碳水化合物(葡萄糖、果糖等)，碳水化合物是活细胞的主要能量来源。到目前为止已鉴定的14个人臀部具有相似的序列，但具有不同的底物特异性和组织分布。 糖尿病患者GLUT2、GLUT2、GLU4和GLU5的活性或/和定位受到影响。谷氨酸配体用于癌症的诊断成像，并正在成为治疗人类癌症的新替代品。 尽管谷氨酸具有压倒一切的重要性，但目前还没有关于任何人类葡萄糖转运蛋白或其同系物的三维结构信息。确定任何供过于求的3D结构将是这一基本运输系统研究的重大突破，并将开辟新的研究途径。