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实现强效且安全的抗菌肽的发现与虚拟筛选。抗菌活性和细胞毒性的同时预测。

Enabling the Discovery and Virtual Screening of Potent and Safe Antimicrobial Peptides. Simultaneous Prediction of Antibacterial Activity and Cytotoxicity.

作者信息

Kleandrova Valeria V, Ruso Juan M, Speck-Planche Alejandro, Dias Soeiro Cordeiro M Natália

机构信息

Faculty of Technology and Production Management, Moscow State University of Food Production , Volokolamskoe shosse 11, Moscow, Russia.

Department of Applied Physics, University of Santiago de Compostela (USC) , 15782 Santiago de Compostela, Spain.

出版信息

ACS Comb Sci. 2016 Aug 8;18(8):490-8. doi: 10.1021/acscombsci.6b00063. Epub 2016 Jul 1.

Abstract

Antimicrobial peptides (AMPs) represent promising alternatives to fight against bacterial pathogens. However, cellular toxicity remains one of the main concerns in the early development of peptide-based drugs. This work introduces the first multitasking (mtk) computational model focused on performing simultaneous predictions of antibacterial activities, and cytotoxicities of peptides. The model was created from a data set containing 3592 cases, and it displayed accuracy higher than 96% for classifying/predicting peptides in both training and prediction (test) sets. The technique known as alanine scanning was computationally applied to illustrate the calculation of the quantitative contributions of the amino acids (in their respective positions of the sequence) to the biological effects of a defined peptide. A small library formed by 10 peptides was generated, where peptides were designed by considering the interpretations of the different descriptors in the mtk-computational model. All the peptides were predicted to exhibit high antibacterial activities against multiple bacterial strains, and low cytotoxicity against various cell types. The present mtk-computational model can be considered a very useful tool to support high throughput research for the discovery of potent and safe AMPs.

摘要

抗菌肽(AMPs)是对抗细菌病原体的有前景的替代物。然而,细胞毒性仍然是基于肽的药物早期开发中的主要关注点之一。这项工作引入了首个多任务(mtk)计算模型,该模型专注于同时预测肽的抗菌活性和细胞毒性。该模型由一个包含3592个案例的数据集创建而成,在训练集和预测(测试)集中对肽进行分类/预测时,其准确率高于96%。通过计算应用称为丙氨酸扫描的技术,以说明氨基酸(在序列中的各自位置)对特定肽的生物学效应的定量贡献的计算。生成了一个由10种肽组成的小型文库,其中肽的设计考虑了mtk计算模型中不同描述符的解释。预计所有这些肽对多种细菌菌株均表现出高抗菌活性,对各种细胞类型的细胞毒性较低。当前的mtk计算模型可被视为支持高通量研究以发现强效且安全的抗菌肽的非常有用的工具。

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