STRUCTURE DETERMINATION OF MEMBRANE-INTEGRATING FORMS OF BCL-2 PROTEINS

BCL-2 蛋白膜整合形式的结构测定

• 批准号: 8170170
• 负责人: Tarmo Roosild
• 金额: $ 0.13万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-01 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8170170
• 关键词: Apoptotic; Cell Membrane Permeability; Cessation of life; Chemistry; Computer Retrieval of Information on Scientific Projects Database; Crystallization; Data; Detergents; Disease; Funding; Grant; Institution; Malignant Neoplasms; Mediating; Medicine; Membrane; Membrane Proteins; Mitochondria; Molecular; Molecular Conformation; Pathway interactions; Pharmaceutical Preparations; Process; Proteins; Research; Research Personnel; Resolution; Resources; Roentgen Rays; Source; Structure; Techniques; Technology; United States National Institutes of Health; design; improved; insight; novel; novel strategies; programs; protein expression; protein function; research study

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The experiments proposed under this program will produce new insights into our understanding of the molecular mechanisms by which Bcl-2 proteins regulate the mitochondria-mediated apoptotic pathway and suggest new approaches to therapeutically modulating this process when aberrant in cancer and other diseases. We will use the Mistic protein expression technology to produce Bcl-2 proteins in active, membrane-integrated conformations at quantities sufficient for structural analysis. Advances in detergent chemistry and membrane protein crystallization techniques will facilitate high resolution X-ray structure determination of these critical apoptotic regulators in their functional conformations. This structural data will greatly improve our understanding of the means by which these proteins control mitochondria membrane permeability to regulate cellular death pathways. Greater insight into the structural mechanisms underlying the function of these proteins when in their active, membrane-integrated conformations will substantially aid the rational design of improved drugs and novel medicines for a broad variety of illnesses.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。列出的机构为 研究中心，而研究中心不一定是研究者所在的机构。 根据该计划提出的实验将产生新的见解，我们的理解的分子机制，Bcl-2蛋白调节的细胞凋亡途径，并建议新的方法来治疗调节这一过程时，异常的癌症和其他疾病。我们将使用Mistic蛋白表达技术以足以进行结构分析的数量生产活性膜整合构象的Bcl-2蛋白。洗涤剂化学和膜蛋白结晶技术的进展将促进这些关键的凋亡调节剂在其功能构象的高分辨率X射线结构测定。这些结构数据将大大提高我们对这些蛋白质控制线粒体膜通透性以调节细胞死亡途径的理解。更深入地了解这些蛋白质在处于活性、膜整合构象时功能的结构机制，将大大有助于合理设计用于多种疾病的改进药物和新药。