Suppr超能文献

“靶向”搜索:一个升级的抗菌肽结构和功能数据库,用于生物膜研究(B-AMP v2.0),重点是生物膜蛋白靶标。

'Targeting' the search: An upgraded structural and functional repository of antimicrobial peptides for biofilm studies (B-AMP v2.0) with a focus on biofilm protein targets.

机构信息

Department of Bioinformatics, School of Chemical and Biotechnology, SASTRA Deemed to be University, Thanjavur, India.

Remote internship with Human Relevant Infection Biology Group, Pune, India.

出版信息

Front Cell Infect Microbiol. 2022 Oct 18;12:1020391. doi: 10.3389/fcimb.2022.1020391. eCollection 2022.

Abstract

Bacterial biofilms, often as multispecies communities, are recalcitrant to conventional antibiotics, making the treatment of biofilm infections a challenge. There is a push towards developing novel anti-biofilm approaches, such as antimicrobial peptides (AMPs), with activity against specific biofilm targets. In previous work, we developed Biofilm-AMP, a structural and functional repository of AMPs for biofilm studies (B-AMP v1.0) with more than 5000 structural models of AMPs and a vast library of AMP annotations to existing biofilm literature. In this study, we present an upgraded version of B-AMP, with a focus on existing and novel bacterial biofilm targets. B-AMP v2.0 hosts a curated collection of 2502 biofilm protein targets across 473 bacterial species, with structural protein models and functional annotations from PDB, UniProt, and PubMed databases. The biofilm targets can be searched for using the name of the source organism, and function and type of protein, and results include designated Target IDs (unique to B-AMP v2.0), UniProt IDs, 3D predicted protein structures, PDBQT files, pre-defined protein functions, and relevant scientific literature. To present an example of the combined applicability of both, the AMP and biofilm target libraries in the repository, we present two case studies. In the first case study, we expand an pipeline to evaluate AMPs against a single biofilm target in the multidrug resistant, bacterial pathogen , using 3D protein-peptide docking models from previous work and Molecular Dynamics simulations (~1.2µs). In the second case study, we build an pipeline to identify candidate AMPs (using AMPs with both anti-Gram positive and anti-Gram negative activity) against two biofilm targets with a common functional annotation in and , widely-encountered bacterial co-pathogens. With its enhanced structural and functional capabilities, B-AMP v2.0 serves as a comprehensive resource for AMP investigations related to biofilm studies. B-AMP v2.0 is freely available at https://b-amp.karishmakaushiklab.com and will be regularly updated with structural models of AMPs and biofilm targets, as well as 3D protein-peptide interaction models for key biofilm-forming pathogens.

摘要

细菌生物膜通常是多菌种群落,对传统抗生素具有抗性,因此治疗生物膜感染具有挑战性。目前人们正在积极开发新型抗生物膜方法,例如针对特定生物膜靶标的抗菌肽 (AMP)。在之前的工作中,我们开发了 Biofilm-AMP,这是一个用于生物膜研究的 AMP 结构和功能存储库 (B-AMP v1.0),其中包含超过 5000 种 AMP 的结构模型和针对现有生物膜文献的 AMP 注释的大型文库。在这项研究中,我们展示了 B-AMP 的升级版,重点是现有的和新型的细菌生物膜靶标。B-AMP v2.0 提供了经过精心整理的 473 种细菌物种的 2502 种生物膜蛋白靶标,这些靶标具有来自 PDB、UniProt 和 PubMed 数据库的结构蛋白模型和功能注释。可以使用来源生物体的名称、蛋白质的功能和类型来搜索生物膜靶标,结果包括指定的 Target IDs(B-AMP v2.0 独有的)、UniProt IDs、3D 预测蛋白结构、PDBQT 文件、预定义的蛋白功能和相关科学文献。为了展示存储库中 AMP 和生物膜靶标库的综合适用性,我们提供了两个案例研究。在第一个案例研究中,我们扩展了一个 管道,使用来自以前工作的 3D 蛋白-肽对接模型和分子动力学模拟 (~1.2µs) 评估针对多药耐药性细菌病原体中单个生物膜靶标的 AMP。在第二个案例研究中,我们构建了一个 管道,以识别针对 和 中具有共同功能注释的两个生物膜靶标的候选 AMP(使用对革兰氏阳性和革兰氏阴性均具有活性的 AMP),这两种生物膜靶标是广泛遇到的细菌共病原体。随着其增强的结构和功能能力,B-AMP v2.0 成为与生物膜研究相关的 AMP 研究的综合资源。B-AMP v2.0 可在 https://b-amp.karishmakaushiklab.com 免费获得,并将定期更新 AMP 和生物膜靶标的结构模型,以及针对关键生物膜形成病原体的 3D 蛋白-肽相互作用模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a86/9623296/2542f4f4a4af/fcimb-12-1020391-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验