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首页> 外文期刊>IEEE transactions on evolutionary computation >Protein Folding in Simplified Models With Estimation of Distribution Algorithms
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Protein Folding in Simplified Models With Estimation of Distribution Algorithms

机译:简化模型中蛋白质折叠的分布算法估计

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摘要

Simplified lattice models have played an important role in protein structure prediction and protein folding problems. These models can be useful for an initial approximation of the protein structure, and for the investigation of the dynamics that govern the protein folding process. Estimation of distribution algorithms (EDAs) are efficient evolutionary algorithms that can learn and exploit the search space regularities in the form of probabilistic dependencies. This paper introduces the application of different variants of EDAs to the solution of the protein structure prediction problem in simplified models, and proposes their use as a simulation tool for the analysis of the protein folding process. We develop new ideas for the application of EDAs to the bidimensional and tridimensional (2-d and 3-d) simplified protein folding problems. This paper analyzes the rationale behind the application of EDAs to these problems, and elucidates the relationship between our proposal and other population-based approaches proposed for the protein folding problem. We argue that EDAs are an efficient alternative for many instances of the protein structure prediction problem and are indeed appropriate for a theoretical analysis of search procedures in lattice models. All the algorithms introduced are tested on a set of difficult 2-d and 3-d instances from lattice models. Some of the results obtained with EDAs are superior to the ones obtained with other well-known population-based optimization algorithms.
机译:简化的晶格模型在蛋白质结构预测和蛋白质折叠问题中发挥了重要作用。这些模型可用于蛋白质结构的初始近似,以及用于研究控制蛋白质折叠过程的动力学。分布算法(EDA)的估计是一种高效的进化算法,可以以概率依赖性的形式学习和利用搜索空间的规律性。本文介绍了EDA的不同变体在简化模型中蛋白质结构预测问题的解决方案中的应用,并提出了将其用作模拟工具来分析蛋白质折叠过程的方法。我们为将EDA应用于二维和三维(2-d和3-d)简化的蛋白质折叠问题开发了新思路。本文分析了将EDA用于这些问题的基本原理,并阐明了我们的建议与针对蛋白质折叠问题提出的其他基于人群的方法之间的关系。我们认为,EDA是蛋白质结构预测问题的许多实例的有效替代方法,确实适用于晶格模型中搜索程序的理论分析。引入的所有算法均在来自晶格模型的一组困难的2维和3维实例上进行了测试。使用EDA获得的某些结果优于通过其他众所周知的基于总体的优化算法获得的结果。

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