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重新审视格子蛋白结构预测。

On lattice protein structure prediction revisited.

机构信息

Biology Department, Boston College, Higgins 355, 140 Commonwealth Avenue, Chestnut Hill, MA 02467, USA.

出版信息

IEEE/ACM Trans Comput Biol Bioinform. 2011 Nov-Dec;8(6):1620-32. doi: 10.1109/TCBB.2011.41.

Abstract

Protein structure prediction is regarded as a highly challenging problem both for the biology and for the computational communities. In recent years, many approaches have been developed, moving to increasingly complex lattice models and off-lattice models. This paper presents a Large Neighborhood Search (LNS) to find the native state for the Hydrophobic-Polar (HP) model on the Face-Centered Cubic (FCC) lattice or, in other words, a self-avoiding walk on the FCC lattice having a maximum number of H-H contacts. The algorithm starts with a tabu-search algorithm, whose solution is then improved by a combination of constraint programming and LNS. The flexible framework of this hybrid algorithm allows an adaptation to the Miyazawa-Jernigan contact potential, in place of the HP model, thus suggesting its potential for tertiary structure prediction. Benchmarking statistics are given for our method against the hydrophobic core threading program HPstruct, an exact method which can be viewed as complementary to our method.

摘要

蛋白质结构预测是生物学和计算科学界都面临的一个极具挑战性的问题。近年来,已经开发出了许多方法,这些方法逐渐向越来越复杂的格子模型和非格子模型转移。本文提出了一种大邻域搜索(LNS)方法,用于在面心立方(FCC)格子上找到疏水-极性(HP)模型的天然状态,或者换句话说,就是在 FCC 格子上进行最大数量的 H-H 接触的自回避行走。该算法从禁忌搜索算法开始,然后通过约束编程和 LNS 的组合来改进其解决方案。这种混合算法的灵活框架允许适应 Miyazawa-Jernigan 接触势能,而不是 HP 模型,从而为三级结构预测提供了可能性。针对我们的方法,给出了与疏水核心穿线程序 HPstruct 的基准测试统计数据,HPstruct 是一种精确的方法,可以视为与我们的方法互补。

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