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Subcellular location prediction of apoptosis proteins using two novel feature extraction methods based on evolutionary information and LDA

机译:基于进化信息和LDA的两种新特征提取方法预测凋亡蛋白的亚细胞定位

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摘要

Apoptosis, also known as programmed cell death, is a basic biological phenomenon that is associated with the occurrence of a wide variety of diseases, such as a tumor, autoimmune disease, Alzheimer’s disease and so on. It plays an important role in animal development and homeostasis [ ]. Studies have shown that apoptosis proteins are essential in this process. The subcellular location of a protein is closely related to its function. And only in the specific subcellular location, can the protein work [ ]. Subcellular localization information of apoptosis proteins contributes to exploring the internal mechanism of programmed cell death and designing new drugs [ ]. However, the number of apoptosis proteins with clear subcellular location markers is limited in the database, and it is time-consuming and costly to label samples by traditional experimental methods. Therefore, exploring feasible computational methods to predict the subcellular location of the given protein has been a hotspot for nearly two decades.
机译:凋亡,也称为程序性细胞死亡,是一种基本的生物学现象,与多种疾病的发生有关,例如肿瘤,自身免疫性疾病,阿尔茨海默氏病等。它在动物发育和体内平衡中起着重要作用[]。研究表明,凋亡蛋白在此过程中至关重要。蛋白质的亚细胞位置与其功能密切相关。而且只有在特定的亚细胞位置,蛋白质才能起作用[]。凋亡蛋白的亚细胞定位信息有助于探索程序性细胞死亡的内部机制和设计新药物[]。然而,在数据库中具有清晰的亚细胞定位标记的凋亡蛋白的数量是有限的,并且通过传统的实验方法标记样品既费时又昂贵。因此,探索可行的计算方法以预测给定蛋白质的亚细胞位置一直是近二十年来的热点。

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