BACTERIAL CHAPERONIN MACHINES

细菌伴侣机器

• 批准号: 7357796
• 负责人: DAVID T CHUANG
• 金额: $ 1.51万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-12-01 至 2006-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7357796
• 关键词: BACTERIAL; CHAPERONIN; MACHINES

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. Chaperonins function by interacting with nascent or unfolded polypeptides to prevent misfolding, which otherwise leads to aggregation. Bacterial chaperonins GroEL/GroES are homologues of mitochondrial Hsp60/Hsp10, respectively. GroEL is a 14-meric double-ring complex of 800 kDa in size, whereas its co-chaperonin GroES is a 70-kDa 7-meric single-ring complex. The mechanism by which molecular chaperones promote proper folding is of intense interest. However, most studies have used small proteins or synthetic peptides as model substrates. Limited information is available as to how these chaperones mediate folding and/or assembly of hetero-oligomeric proteins or macromolecular structures. To understand the mechanism underlying chaperonin-assisted protein folding and assembly, we plan to dp the following cryo-EM studies. Specific Aims: 1. To continue using the GroEL double-ring complex as a model for cryo-EM reconstruction with the goal of attaining 4-¿ resolution. 2. To determine three-dimensional structures of single ring mutant of GroEL bound with subs

该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者（PI）可能从另一个NIH来源获得主要资金，因此可以在其他CRISP条目中表示。所列机构为中心，不一定是研究者所在机构。伴侣蛋白通过与新生或未折叠的多肽相互作用以防止错误折叠而起作用，否则错误折叠会导致聚集。细菌伴侣蛋白GroEL/GroES分别是线粒体Hsp 60/Hsp 10的同源物。GroEL是一个大小为800 kDa的14梅里克双环复合物，而其辅伴侣GroES是一个70 kDa的7梅里克单环复合物。分子伴侣促进正确折叠的机制引起了人们的强烈兴趣。然而，大多数研究使用小蛋白或合成肽作为模型底物。关于这些分子伴侣如何介导异源寡聚蛋白质或大分子结构的折叠和/或组装的信息有限。为了了解伴侣蛋白辅助蛋白质折叠和组装的机制，我们计划进行以下冷冻电镜研究。 具体目标：1。继续使用GroEL双环复合体作为冷冻EM重建模型，目标是达到4-½分辨率。2.确定GroEL单环突变体与亚基结合的三维结构，