HEMOGLOBIN STRUCTURE-FUNCTION & BLOOD SUBSTITUTE DESIGN

血红蛋白结构-功能

• 批准号: 2028991
• 负责人: Gary K Ackers
• 金额: $ 110.87万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1993
• 资助国家: 美国
• 起止时间: 1993-12-01 至 1998-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/2028991
• 关键词: blood /plasma substitute; hemoglobin; hemoprotein structure; protein structure function

The central goal is to develop a better understanding of the factors and elements which control functional behavior of the human hemoglobin molecule. The approach that will be employed is to identify the roles of amino acid side chains in the molecule's normal functioning by residue substitution at specifically targeted sites coupled with extensive structural and functional characterization of the resulting hemoglobin molecules. This Program Project brings together seven research groups that have complementary areas of expertise and a common focus of interest on mechanisms of hemoglobin function and structure. In order to achieve this concentrated effort, it has been necessary to bring together individuals from a number of different institutions. (We know of no single institution with a comparable level of interest and expertise in this field.) This group has a proven track record of productive collaboration during the previous period of this grant. Other strengths include: a) efficiently functioning core facilities that have been developed under the current funding of this Program Project for production of large amounts of genetically engineered hemoglobin variants. b) Facilities and expertise for detailed, systematic characterization of structural (i.e., x-ray, spectroscopic, and theoretical) and functional (kinetic and thermodynamic) properties of hemoglobin. Work in the different laboratories will be coordinated through planned collaborations, exchanges of materials and personnel, and quarterly meetings. Results will be synthesized into a predictive model of the hemoglobin mechanism. This new level of understanding may permit the rational design of structurally-modified hemoglobins with desired properties, including potential red cell substitute materials.

中心目标是更好地了解这些因素， 控制人类血红蛋白功能行为的元素 分子。将采用的方法是确定以下方面的作用： 氨基酸在分子侧链上的正常功能由残基 在特定靶位点的取代加上广泛的 所得血红蛋白的结构和功能表征 分子。 该项目汇集了七个研究小组， 互补的专业知识领域和共同关注的重点 血红蛋白功能和结构的机制。为了实现这一 集中精力，有必要将个人聚集在一起， 来自不同的机构。(We据我所知， 在这一领域的兴趣和专业知识水平相当）。这 集团在2015年期间拥有富有成效的合作记录 在此期间，该补助金。其他优点包括：a）效率高 在目前的情况下开发的功能核心设施 该计划项目的资金用于生产大量的 基因工程血红蛋白变体。B）设施和专门知识 为了详细、系统地表征结构（即，X射线， 光谱和理论）和功能（动力学和热力学） 血红蛋白的性质。 不同实验室的工作将通过计划的 合作、物资和人员交流， 会议.结果将被合成为一个预测模型， 血红蛋白机制这种新的理解水平可能允许 具有所需结构修饰的血红蛋白的合理设计 包括潜在的红细胞替代材料。