Monitoring Biomolecular Interactions using Isothermal Titration Calorimetry

使用等温滴定量热法监测生物分子相互作用

• 批准号: 439546-2013
• 负责人: Jia, Zongchao
• 金额: $ 8.6万
• 依托单位: Queen's University
• 依托单位国家: 加拿大
• 项目类别: Research Tools and Instruments - Category 1 (<$150,000)
• 财政年份: 2012
• 资助国家: 加拿大
• 起止时间: 2012-01-01 至 2013-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=505647
• 关键词: Monitoring; Biomolecular; Interactions; using; Isothermal

The proper functioning of a protein is intimately associated with its ability to recognize and bind to specific target molecules at the right time and with the right affinity. The applicants' research interests are diverse, but nonetheless converge on to the characterization of proteins and their interactions with target molecules such as ions, metal co-factors, small molecules and other proteins in health and disease. To gain a more comprehensive understanding of these interactions one requires detailed knowledge about the associated macromolecular parameters such as the strength, the number of molecules involved, and various energetic coefficients. Isothermal titration calorimetry (ITC) is a proven and robust biophysical methodology that can directly measure these parameters in solution. Moreover, ITC is attractive because it does not require modification of the molecules under investigation, which can potentially disrupt the extent of interaction. Technical advances in ITC design have allowed for significantly reduced sample volumes, allowing for direct measurement of protein-ligand interactions in solution using a microcalorimeter. We are requesting such a device to fulfill a pressing need to explore the structural, biophysical and chemical basis of novel protein interactions at Queen's University. Data derived from these experiments will lead to an improved understanding of their role in cellular function and regulation. Funding of this proposal will provide a continuing opportunity for the high-qualified personnel (HQP) to gain valuable training with one of the most widely used approaches in modern protein structure and function studies. This work will not only expand HQP training and collaborative work in this area of research, but will also position the applicants in making key discoveries that have broader implications in the fields of green chemistry, cellular regulation, and agriculture.

蛋白质的正常功能与其在正确的时间以正确的亲和力识别和结合特定靶分子的能力密切相关。申请人的研究兴趣是多样的，但仍然集中在蛋白质的表征及其与靶分子的相互作用，如离子，金属辅因子，小分子和健康和疾病中的其他蛋白质。为了更全面地了解这些相互作用，需要详细了解相关的大分子参数，如强度，所涉及的分子数量和各种能量系数。 等温滴定量热法（ITC）是一种成熟可靠的生物物理方法，可以直接测量溶液中的这些参数。此外，ITC是有吸引力的，因为它不需要对正在研究的分子进行修饰，这可能会破坏相互作用的程度。ITC设计的技术进步使得样品体积大大减少，从而可以使用微量热计直接测量溶液中的蛋白质-配体相互作用。我们要求这样的设备，以满足迫切需要探索结构，生物物理和化学基础上的新蛋白质相互作用在皇后大学。从这些实验中获得的数据将有助于更好地理解它们在细胞功能和调节中的作用。该提案的资助将为高素质人员（HQP）提供持续的机会，以获得现代蛋白质结构和功能研究中最广泛使用的方法之一的宝贵培训。 这项工作不仅将扩大HQP培训和合作工作在这一领域的研究，但也将定位申请人在作出关键发现，有更广泛的影响领域的绿色化学，细胞调控和农业。