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An improved parallel differential evolution approach for protein structure prediction using both 2D and 3D off-lattice models

机译:使用2D和3D非晶格模型的蛋白质结构预测的改进的并行差分进化方法

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Protein structure prediction (PSP) is a well-known problem in bioinformatics. Identifying protein native conformations makes it possible to predict its function within the organism. Knowing this also helps the development of new drugs and the comprehension of some biological mechanisms. During years some techniques have been developed for this purpose but, due to their high cost, it is necessary to use simplified models of protein structures. However, even the simplest models, with low biological plausibility, are excessively complex from the computational point of view. This paper reports the application of Differential Evolution (DE) to solve the PSP problem using a Toy Model (also known as the AB Model) in both 2D and 3D to represent the protein structure. This work presents two different versions of the DE algorithm (basic and adaptive) using a parallel architecture (master-slave) based on Message Passing Interface in a cluster. Some special operators for DE were developed: explosion and mirror mutation. All tests executed in this work used four benchmark sequences, ranging from 13 to 55 amino acids. The results for both parallel DE algorithms using both 2D and 3D models were compared with other works in the literature. The DE algorithm achieved excellent results. Overall results encourage further research towards the use of knowledge-based operators to improve further the performance of DE.
机译:蛋白质结构预测(PSP)是生物信息学中的一个众所周知的问题。鉴定蛋白质天然构象可以预测其在生物体内的功能。知道这一点还有助于开发新药和理解某些生物学机制。多年来,已经为此目的开发了一些技术,但是由于它们的高成本,有必要使用简化的蛋白质结构模型。但是,从计算的角度来看,即使是最简单的模型,其生物学可信度也很低。本文报告了在2D和3D中使用玩具模型(也称为AB模型)来代表蛋白质结构的差异进化(DE)在解决PSP问题中的应用。这项工作使用基于集群中消息传递接口的并行体系结构(主从),提出了两种不同版本的DE算法(基本和自适应)。开发了一些特殊的DE运算符:爆炸和镜像突变。在这项工作中执行的所有测试都使用四个基准序列,范围从13到55个氨基酸。使用2D和3D模型的两种并行DE算法的结果都与文献中的其他作品进行了比较。 DE算法取得了优异的效果。总体结果鼓励对使用基于知识的运算符进行进一步研究以进一步提高DE的性能。

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