4.6 Article

ABP-Finder: A Tool to Identify Antibacterial Peptides and the Gram-Staining Type of Targeted Bacteria

期刊

ANTIBIOTICS-BASEL
卷 11, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/antibiotics11121708

关键词

antibacterial peptide; machine learning; AMPs database; StarPep; Gram staining-based target; peptide library screening; human peptidome

资金

  1. German Research Foundation (DFG) [316249678, CRC 1279, EXC 2033-390677874-RESOLV, 436586093, CRC 1430, 424228829]
  2. Portuguese Foundation for Science and Technology (Fundacao para a Ciencia e a Tecnologia-FCT) [UIDB/04423/2020, UIDP/04423/2020]

向作者/读者索取更多资源

The problem of multi-drug resistance in bacteria is a major global health issue. Peptides, which have binding specificity and low side effects, are seen as promising candidates for the development of new antibiotics. However, there is a lack of tools that can consistently predict the antibacterial activity of peptides. In this study, a new tool called ABP-Finder was introduced, which can identify antibacterial peptides and estimate the susceptibility of bacteria to their action. The tool ranks highly in terms of precision and has been successfully applied to screen a large peptide library and identify an antibacterial peptide.
Multi-drug resistance in bacteria is a major health problem worldwide. To overcome this issue, new approaches allowing for the identification and development of antibacterial agents are urgently needed. Peptides, due to their binding specificity and low expected side effects, are promising candidates for a new generation of antibiotics. For over two decades, a large diversity of antimicrobial peptides (AMPs) has been discovered and annotated in public databases. The AMP family encompasses nearly 20 biological functions, thus representing a potentially valuable resource for data mining analyses. Nonetheless, despite the availability of machine learning-based approaches focused on AMPs, these tools lack evidence of successful application for AMPs' discovery, and many are not designed to predict a specific function for putative AMPs, such as antibacterial activity. Consequently, among the apparent variety of data mining methods to screen peptide sequences for antibacterial activity, only few tools can deal with such task consistently, although with limited precision and generally no information about the possible targets. Here, we addressed this gap by introducing a tool specifically designed to identify antibacterial peptides (ABPs) with an estimation of which type of bacteria is susceptible to the action of these peptides, according to their response to the Gram-staining assay. Our tool is freely available via a web server named ABP-Finder. This new method ranks within the top state-of-the-art ABP predictors, particularly in terms of precision. Importantly, we showed the successful application of ABP-Finder for the screening of a large peptide library from the human urine peptidome and the identification of an antibacterial peptide.

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