Using distance geometry algorithms to derive molecular conformational ensembles

使用距离几何算法导出分子构象系综

• 批准号: 8564-2011
• 负责人: Burkowski, Forbes
• 金额: $ 1.02万
• 依托单位: University of Waterloo
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2014
• 资助国家: 加拿大
• 起止时间: 2014-01-01 至 2015-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=544534
• 关键词: Using; distance; geometry; algorithms; derive

Motivation: When a ligand (such as a drug molecule) docks with the binding site of a protein, both molecules undergo conformational changes. These changes are difficult to predict and this complicates the necessary geometric modeling of the final combined structure. To simplify the analysis, a drug designer may make the over-optimistic assumption that the binding site is rigid and flexibility is only considered for the ligand. A more complicated analysis deals with the flexibility of both the ligand and the binding site: We consider conformational changes in the binding site to be small deviations from the structure that corresponds to the lowest energy conformation of the protein. This "induced fit hypothesis" provides a more realistic account of the docking event. Nonetheless, it is not fully adequate and there are many protein-ligand complexes in which the binding site has undergone extensive conformational changes. Recently, various researchers have devised more complicated geometrical descriptions in an effort to more fully capture the complexity of a binding event. These studies assume that the protein is usually in a low energy conformation but, due to thermal agitation or crowding, it may occasionally adopt a different conformation that corresponds to a nearby local energy minimum at the bottom of the "folding funnel". This conformation would have an energy that is only slightly larger when compared with the energy of the global minimum. The physical presence of this "conformational ensemble" greatly complicates any attempt to build predictive machine learning algorithms for drug design efforts because it is difficult to collect training data that provides enough samples for each of the unknown conformations. Our goal is to study the geometrical modeling of binding sites with the goal of devising algorithms for the generation of conformational ensembles as a prelude to ligand docking.

动机：当配体（如药物分子）与蛋白质的结合位点对接时，两个分子都发生构象变化。 这些变化很难预测，这使得最终组合结构的必要几何建模复杂化。 为了简化分析，药物设计者可能会做出过于乐观的假设，即结合位点是刚性的，而柔性只考虑配体。 一个更复杂的分析涉及配体和结合位点的灵活性：我们认为结合位点的构象变化是与蛋白质最低能量构象对应的结构的微小偏差。 这个“诱导契合假说”提供了一个更现实的对接事件的帐户。 然而，这是不完全足够的，有许多蛋白质-配体复合物中的结合位点经历了广泛的构象变化。 最近，各种研究人员设计了更复杂的几何描述，以更全面地捕捉结合事件的复杂性。 这些研究假设蛋白质通常处于低能量构象，但是由于热搅动或拥挤，它可能偶尔采用与“折叠漏斗”底部附近的局部能量最小值相对应的不同构象。 这种构象的能量与全局最小值的能量相比只稍微大一点。 这种“构象集合”的物理存在极大地复杂化了为药物设计工作构建预测机器学习算法的任何尝试，因为难以收集为每个未知构象提供足够样本的训练数据。 我们的目标是研究结合位点的几何建模，目标是设计用于生成构象集合的算法，作为配体对接的前奏。