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统一抗菌肽数据库中的抗菌肽分类。

Unifying the classification of antimicrobial peptides in the antimicrobial peptide database.

机构信息

Department of Pathology and Microbiology, College of Medicine, University of Nebraska Medical Center, 985900 Nebraska Medical Center, Omaha, NE, United States.

出版信息

Methods Enzymol. 2022;663:1-18. doi: 10.1016/bs.mie.2021.09.006. Epub 2021 Oct 12.

Abstract

Natural products offer an important avenue to novel therapeutics against drug-resistant bacteria, viruses, fungi, parasites, and cancer. However, there are numerous hurdles and challenges in discovering such molecules, including antimicrobial peptides (AMPs). While a thorough characterization of AMPs is limited by the amount of material, existing technology, and researcher's expertise, peptide classification is complicated by incomplete information as well as different methods proposed for AMPs from bacteria, plants, and animals. This article describes unified classification schemes for natural AMPs on a common platform: the Antimicrobial Peptide Database (APD; https://aps.unmc.edu). The various criteria for these unified classifications include peptide biological source, biosynthesis machinery, biological activity, amino acid sequence, mechanism of action, and three-dimensional structure. To overcome the problem with a limited number of known 3D structures, a universal peptide classification has also been refined and executed in the APD database. This universal method, based on the spatial connection patterns of polypeptide chains, is independent of peptide source, size, activity, 3D structure, or mechanism of action. It facilitates information registration, naming, exchange, decoding, prediction, and design of novel antimicrobial peptides.

摘要

天然产物为治疗耐药细菌、病毒、真菌、寄生虫和癌症提供了重要途径。然而,在发现这些分子时存在许多障碍和挑战,包括抗菌肽(AMPs)。虽然对 AMPs 的全面表征受到材料数量、现有技术和研究人员专业知识的限制,但由于信息不完整以及从细菌、植物和动物中提出的 AMPs 的不同方法,肽分类变得复杂。本文描述了天然 AMPs 在通用平台上的统一分类方案:抗菌肽数据库(APD;https://aps.unmc.edu)。这些统一分类的各种标准包括肽的生物来源、生物合成机制、生物活性、氨基酸序列、作用机制和三维结构。为了克服已知 3D 结构数量有限的问题,还在 APD 数据库中对通用肽分类进行了改进和执行。这种基于多肽链空间连接模式的通用方法独立于肽源、大小、活性、3D 结构或作用机制。它促进了新型抗菌肽的信息注册、命名、交换、解码、预测和设计。

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