TM INTERACTIONS IN MEMBRANE PROTEIN FOLDING AND FUNCTION

膜蛋白折叠和功能中的 TM 相互作用

• 批准号: 7036105
• 负责人: DONALD M. ENGELMAN
• 金额: $ 43.35万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-05-15 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7036105
• 关键词: HIV envelope protein gp41; MHC class I antigen; SDS polyacrylamide gel electrophoresis; analytical ultracentrifugation; biological signal transduction; cell membrane; chemical bond; computational biology; computer simulation; fluorescence resonance energy transfer; membrane activity; membrane proteins; membrane structure; micelles; nuclear magnetic resonance spectroscopy; optics; polymers; protein folding; protein protein interaction; protein structure; spectrometry

DESCRIPTION (provided by applicant): Interactions between transmembrane helices are a major feature of the architecture of membrane proteins. Understanding the principles that guide such interactions will illuminate membrane protein folding, stability, and oligomer formation. Since membrane proteins are coded by more than 20% of all genes and are the targets of more than half of all drugs, such an understanding will be both enlightening and useful. We will work towards understanding the motifs and interactions that give rise to transmembrane helix (TM) interactions that stabilize protein structures in biological membranes, and to begin to connect our understanding to biological functions. We have developed a diverse toolkit for the study of TM interactions, including: (a) genetic and biochemical assays in micelles, bilayers and membranes, (b) computational approaches, and (c) structural studies using optical spectroscopy and NMR. Our approach will have several major divisions: a study of TM trimers in HIV gp41 TMs and MHC li; an effort to find the link between helix dimerization and signaling; a study of interaction motifs; an improvement of TM-TM computational methods; and tests of the principles and motifs that can be identified in helix associations.

描述（由申请人提供）：跨膜螺旋之间的相互作用是膜蛋白结构的主要特征。了解指导这种相互作用的原理将阐明膜蛋白折叠，稳定性和低聚物形成。由于膜蛋白被所有基因的20％以上编码，并且是所有药物中一半以上的靶标，因此这种理解将是启发性和有用的。我们将致力于理解产生跨膜螺旋（TM）相互作用的基序和相互作用，从而稳定生物膜中的蛋白质结构，并开始将我们的理解与生物学功能联系起来。我们为研究TM相互作用的研究开发了多种工具包，包括：（a）胶束，双层和膜中的遗传和生化测定，（b）计算方法，以及（c）使用光谱光谱和NMR的结构研究。我们的方法将有几个主要分歧：对HIV GP41 TMS和MHC LI中的TM三聚体的研究；努力找到螺旋二聚化和信号传导之间的联系；相互作用图案的研究； TM-TM计算方法的改进；以及可以在Helix关联中识别的原理和基序的测试。