Biophysical Analysis of Enzyme Inhibitor Interactions

酶抑制剂相互作用的生物物理分析

• 批准号: 6899528
• 负责人: Kumar SINNIAH
• 金额: $ 18.9万
• 依托单位: CALVIN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-05-01 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6899528
• 关键词: Biophysical; Analysis; Enzyme; Inhibitor; Interactions

DESCRIPTION (provided by applicant): Understanding enzyme-inhibitor interactions at the molecular level is fundamental to successful drug design. Carbonic anhydrase and its inhibitors provide a robust and prototypic system for developing new methods to study enzyme-ligand interactions. In this study, the technique offeree spectroscopy will be used to investigate enzyme-inhibitor interactions on carbonic anhydrase at the single molecule level. Our long term goal is to examine the capabilities offeree spectroscopy as an analytical tool for a range of enzymes and their inhibitors. The specific aims are designed to: 1. Improve strategies for protein immobilization on surfaces and attaching inhibitors to cantilever probes. An essential requirement for studying biospecific interactions on immobilized surfaces is to present a suitable surface that minimizes non-specific attachments and has a high coverage of the immobilized catalytically active enzyme. To this end, this study will examine several methods for immobilizing the catalytically active carbonic anhydrase with specific control over the orientation of the enzyme. The inhibitor will be attached to a cantilever probe via a flexible linker. 2. Analyze the enzyme-inhibitor interactions by dynamic force spectroscopy. We will quantify the interactions between an oriented carbonic anhydrase enzyme and a sulfonamide inhibitor tethered to an atomic force microscope cantilever. Since the interaction forces are dependent on the loading rate of the cantilever, the loading rate will be varied to map the energy landscape of the enzyme-inhibitor complex. 3. Determine how competitive interactions affect enzyme-inhibitor interactions. We plan to block the active site of the enzyme by introducing other competitive inhibitors, and thereby reduce the specific interactions between the tethered inhibitor and the enzyme. This will provide a method for obtaining inhibitor constants which can be compared to other techniques.

描述（由申请人提供）：在分子水平上理解酶-抑制剂相互作用是成功药物设计的基础。碳酸酐酶及其抑制剂为开发研究酶-配体相互作用的新方法提供了一个强大的原型系统。本研究将利用光谱技术在单分子水平上研究碳酸酐酶与抑制剂的相互作用。我们的长期目标是检验光谱学作为一系列酶及其抑制剂的分析工具的能力。具体目标是： 1.改进蛋白质固定在表面上和将抑制剂附着到悬臂梁探针上的策略。研究固定化表面上的生物特异性相互作用的一个基本要求是提供一种合适的表面，使非特异性附着最小化，并具有固定化催化活性酶的高覆盖率。为此，本研究将探讨几种方法固定的催化活性碳酸酐酶与特定的控制方向的酶。抑制剂将通过柔性接头连接到悬臂探针。 2.动态力谱分析酶-抑制剂相互作用。我们将量化定向碳酸酐酶和磺酰胺抑制剂拴在原子力显微镜悬臂之间的相互作用。由于相互作用力取决于悬臂梁的加载速率，因此加载速率将变化以绘制酶-抑制剂复合物的能量图。 3.确定竞争性相互作用如何影响酶-抑制剂相互作用。我们计划通过引入其他竞争性抑制剂来阻断酶的活性位点，从而减少栓系抑制剂与酶之间的特异性相互作用。这将提供一种获得抑制剂常数的方法，可以与其他技术进行比较。