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增强搜索:抗菌肽的结构和功能资源库用于生物膜研究,及其在新兴病原体 中的应用案例研究。

AMPing Up the Search: A Structural and Functional Repository of Antimicrobial Peptides for Biofilm Studies, and a Case Study of Its Application to , an Emerging Pathogen.

机构信息

Department of Bioinformatics, Guru Nanak Khalsa College of Arts, Science and Commerce (Autonomous), Mumbai, India.

Huck Institutes of Life Sciences, The Pennsylvania State University, University Park, College State, PA, United States.

出版信息

Front Cell Infect Microbiol. 2021 Dec 16;11:803774. doi: 10.3389/fcimb.2021.803774. eCollection 2021.

Abstract

Antimicrobial peptides (AMPs) have been recognized for their ability to target processes important for biofilm formation. Given the vast array of AMPs, identifying potential anti-biofilm candidates remains a significant challenge, and prompts the need for preliminary investigations prior to extensive and studies. We have developed Biofilm-AMP (B-AMP), a curated 3D structural and functional repository of AMPs relevant to biofilm studies. In its current version, B-AMP contains predicted 3D structural models of 5544 AMPs (from the DRAMP database) developed using a suite of molecular modeling tools. The repository supports a user-friendly search, using source, name, DRAMP ID, and PepID (unique to B-AMP). Further, AMPs are annotated to existing biofilm literature, consisting of a vast library of over 10,000 articles, enhancing the functional capabilities of B-AMP. To provide an example of the usability of B-AMP, we use the sortase C biofilm target of the emerging pathogen as a case study. For this, 100 structural AMP models from B-AMP were subject to protein-peptide molecular docking against the catalytic site residues of the sortase C protein. Based on docking scores and interacting residues, we suggest a preference scale using which candidate AMPs could be taken up for further , and testing. The 3D protein-peptide interaction models and preference scale are available in B-AMP. B-AMP is a comprehensive structural and functional repository of AMPs, and will serve as a starting point for future studies exploring AMPs for biofilm studies. B-AMP is freely available to the community at https://b-amp.karishmakaushiklab.com and will be regularly updated with AMP structures, interaction models with potential biofilm targets, and annotations to biofilm literature.

摘要

抗菌肽 (AMPs) 因其能够靶向生物膜形成过程中的重要过程而受到关注。鉴于 AMPs 的种类繁多,识别潜在的抗生物膜候选物仍然是一项重大挑战,并促使在进行广泛研究之前进行初步研究。我们开发了 Biofilm-AMP (B-AMP),这是一个经过精心整理的 3D 结构和功能 AMP 库,与生物膜研究相关。在当前版本中,B-AMP 包含了使用一系列分子建模工具开发的来自 DRAMP 数据库的 5544 个 AMP 的预测 3D 结构模型。该存储库支持使用来源、名称、DRAMP ID 和 PepID(B-AMP 独有的)进行用户友好的搜索。此外,AMPs 被注释到现有的生物膜文献中,其中包含超过 10000 篇文章的庞大库,增强了 B-AMP 的功能能力。为了提供 B-AMP 可用性的示例,我们以新兴病原体的 sortase C 生物膜靶标为例进行研究。为此,从 B-AMP 中选取了 100 个结构 AMP 模型,针对 sortase C 蛋白的催化位点残基进行了蛋白-肽分子对接。根据对接得分和相互作用的残基,我们使用偏好尺度来建议候选 AMP 可以进一步进行研究、实验和验证。3D 蛋白-肽相互作用模型和偏好尺度可在 B-AMP 中获得。B-AMP 是一个综合性的 AMP 结构和功能存储库,将作为未来探索 AMP 用于生物膜研究的基础。B-AMP 可供社区在 https://b-amp.karishmakaushiklab.com 免费获取,并将定期更新 AMP 结构、与潜在生物膜靶标的相互作用模型以及生物膜文献注释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10d5/8716830/2e06f758781c/fcimb-11-803774-g001.jpg

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