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CalCleaveMKL:一种用于钙蛋白酶切割预测的工具。

CalCleaveMKL: a Tool for Calpain Cleavage Prediction.

作者信息

duVerle David A, Mamitsuka Hiroshi

机构信息

Graduate School of Frontier Science, The University of Tokyo, Kashiwa, Chiba, Japan.

Artificial Intelligence Research Center, AIST, Koto-ku, Tokyo, Japan.

出版信息

Methods Mol Biol. 2019;1915:121-147. doi: 10.1007/978-1-4939-8988-1_11.

Abstract

Calpain, an intracellular Ca-dependent cysteine protease, is known to play a role in a wide range of metabolic pathways through limited proteolysis of its substrates. However, only a limited number of these substrates are currently known, with the exact mechanism of substrate recognition and cleavage by calpain still largely unknown.Current sequencing technologies have made it possible to compile large amounts of cleavage data and brought greater understanding of the underlying protein interactions. However, the practical impossibility of exhaustively retrieving substrate sequences through experimentation alone has created the need for efficient computational prediction methods. Such methods must be able to quickly mark substrate candidates and putative cleavage sites for further analysis. While many methods exist for both calpain and other types of proteolytic actions, the expected reliability of these methods depends heavily on the type and complexity of proteolytic action, as well as the availability of well-labeled experimental datasets, which both vary greatly across enzyme families.This chapter introduces CalCleaveMKL: a tool for calpain cleavage prediction based on multiple kernel learning, an extension to the classic support vector machine framework that is able to train complex models based on rich, heterogeneous feature sets, leading to significantly improved prediction quality. Along with its improved accuracy, the method used by CalCleaveMKL provided numerous insights on the respective importance of sequence-related features, such as solvent accessibility and secondary structure. It notably demonstrated there existed significant specificity differences across calpain subtypes, despite previous assumption to the contrary.An online implementation of this prediction tool is available at http://calpain.org .

摘要

钙蛋白酶是一种细胞内钙依赖性半胱氨酸蛋白酶,已知它通过对其底物进行有限的蛋白水解作用,在广泛的代谢途径中发挥作用。然而,目前已知的此类底物数量有限,钙蛋白酶识别和切割底物的确切机制仍很大程度上未知。当前的测序技术使得汇编大量切割数据成为可能,并让人对潜在的蛋白质相互作用有了更深入的理解。然而,仅通过实验详尽检索底物序列在实际中是不可能的,这就产生了对高效计算预测方法的需求。此类方法必须能够快速标记底物候选物和假定的切割位点,以便进一步分析。虽然针对钙蛋白酶和其他类型的蛋白水解作用都存在许多方法,但这些方法的预期可靠性在很大程度上取决于蛋白水解作用的类型和复杂性,以及标记良好的实验数据集的可用性,而这两者在不同酶家族中差异很大。本章介绍了CalCleaveMKL:一种基于多核学习的钙蛋白酶切割预测工具,它是经典支持向量机框架的扩展,能够基于丰富的异构特征集训练复杂模型,从而显著提高预测质量。除了提高准确性之外,CalCleaveMKL所使用的方法还对与序列相关的特征(如溶剂可及性和二级结构)的各自重要性提供了诸多见解。它特别表明,尽管之前有相反的假设,但钙蛋白酶亚型之间存在显著的特异性差异。此预测工具的在线版本可在http://calpain.org上获取。

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