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New hybrid of empirical and knowledge-based scoring functions using novel geometrical descriptors, molecular surface descriptors and machine-learning methods.

机译:使用新颖的几何描述符,分子表面描述符和机器学习方法的新的经验和基于得分函数的混合函数。

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摘要

Protein-ligand interactions are an important and challenging problem in rational drug design. Protein-ligand docking and scoring are essential techniques to study the functions of macromolecular targets and small compounds. Among all scoring functions, knowledge-based scoring functions are the latest and most promising method.; The method described in this thesis is a hybrid of both empirical and knowledge-based scoring functions, In contrast to pair potentials of traditional knowledge-based scoring functions, it applies novel geometrical and molecular surface property descriptors. Like empirical scoring functions, QSAR modeling methods are utilized in this approach. However, this method conceptually considers all the physical effects in protein-ligand interactions, compared to empirical scoring functions.; Three types of descriptors are applied in this approach: atom pair descriptors, TAE/RECON surface property descriptors, and tessellated tetrahedron descriptors. Atom pair descriptors consider the fact that the strength of ligand binding is correlated with the nature of protein-ligand atom pairs in a distance-dependent manner. TAE/RECON descriptors study the surface electronic properties, and find correlations and complementarities between the ligand and protein binding site. Tessellated tetrahedron descriptors investigate the geometrical and molecular properties in the binding site three-dimensional space, and analyze the correlation of this information and the protein-ligand binding energies. All three types of descriptors have obtained reliable scoring and pattern recognition results using bootstrapping mode of Kernel PLS (Partial Least Squares) modeling. Other machine learning methods, such as sensitivity analysis feature selection, Y-scrambling, are involved in our study. The computational results and possible future enhancement are discussed at the end of the thesis.
机译:蛋白质-配体相互作用是合理药物设计中一个重要且具有挑战性的问题。蛋白质-配体对接和评分是研究大分子靶标和小分子化合物功能的基本技术。在所有评分功能中,基于知识的评分功能是最新且最有前途的方法。本文所描述的方法是基于经验的和基于知识的得分函数的混合,与传统的基于知识的得分函数的配对势相反,它应用了新颖的几何和分子表面特性描述符。像经验计分函数一样,此方法中使用了QSAR建模方法。然而,与经验评分函数相比,该方法从概念上考虑了蛋白质-配体相互作用中的所有物理效应。此方法中应用了三种类型的描述符:原子对描述符,TAE / RECON表面特性描述符和棋盘格化四面体描述符。原子对描述子认为配体结合的强度与蛋白质-配体原子对的性质以距离相关的方式相关。 TAE / RECON描述符研究表面电子性质,并发现配体和蛋白质结合位点之间的相关性和互补性。棋盘形四面体描述符研究了结合位点三维空间中的几何和分子特性,并分析了该信息与蛋白质-配体结合能的相关性。使用Kernel PLS(偏最小二乘)建模的自举模式,所有三种类型的描述符都获得了可靠的评分和模式识别结果。我们的研究还涉及其他机器学习方法,例如敏感性分析功能选择,Y-加扰。论文的最后讨论了计算结果和未来可能的改进。

著录项

  • 作者

    Deng, Wei.;

  • 作者单位

    Rensselaer Polytechnic Institute.;

  • 授予单位 Rensselaer Polytechnic Institute.;
  • 学科 Chemistry Organic.; Chemistry Pharmaceutical.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 169 p.
  • 总页数 169
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;药物化学;
  • 关键词

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