UNDERSTANDING THE ARCHITECTURE OF CHALLENGING MULTI-DOMAIN PROTEINS

了解具有挑战性的多域蛋白质的结构

• 批准号: 8170304
• 负责人: ANDREW M GULICK
• 金额: $ 0.03万
• 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/8170304
• 关键词: Amino Acids; Architecture; Binding; Biochemical; Biological Assay; Biological Factors; Catalytic Domain; Cells; Computer Retrieval of Information on Scientific Projects Database; Crystallography; Development; Enzymes; Funding; GRP94; Grant; Heat-Shock Proteins 90; Institution; Investigation; Ligands; Molecular Chaperones; Peptide Antibiotics; Peptides; Proteins; Research; Research Personnel; Resources; Siderophores; Source; Specificity; Tertiary Protein Structure; United States National Institutes of Health; base; novel; peptide synthase; protein function; small molecule

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. This is a proposal describing research into multi-domain and multi-protein assemblies under study in our labs. The Gulick lab is investigating the structural arrangement of non-ribosomal peptide synthetases (NRPSs). These modular proteins catalyze the synthesis of peptides antibiotics and peptide siderophores using amino acid and peptide intermediates that are covalently bound to a carrier domain that delivers substrates to the necessary catalytic domains in a coordinated fashion. The choreography of this assembly line synthesis is being investigated through biochemical studies and structural investigations of multi-domain proteins trapped in catalytically relevant states. Additional projects investigate auxiliary proteins that function with NRPS enzymes in the synthesis of natural products. The Gewirth lab studies the multi-domain HSP90 class of molecular chaperones. Questions at the forefront of the field currently center on the development of inhibitory ligands of high specificity, as well as understanding the mechanistic differences between cytoplasmic Hsp90 and GRP94. We are using x-ray crystallography in combination with biochemical and cell-based assays to study the interaction of the hsp90 family of molecular chaperones with novel small molecule inhibitory ligands.

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。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 这是一个描述我们实验室正在研究的多结构域和多蛋白质组装的研究建议。Gulick实验室正在研究非核糖体肽合成酶（NRPS）的结构排列。这些模块化蛋白质使用与载体结构域共价结合的氨基酸和肽中间体催化肽抗生素和肽铁载体的合成，该载体结构域以协调的方式将底物递送到必要的催化结构域。这种装配线合成的编排正在研究通过生物化学研究和结构研究的多结构域蛋白质被困在催化相关的状态。其他项目研究在天然产物合成中与NRPS酶起作用的辅助蛋白。Gewirth实验室研究多结构域HSP 90类分子伴侣。目前，该领域最前沿的问题集中在开发高特异性的抑制性配体，以及了解细胞质Hsp 90和GRP 94之间的机制差异。我们正在使用x射线晶体学结合生化和细胞为基础的分析，研究热休克蛋白90家族的分子伴侣与新的小分子抑制配体的相互作用。