4.5 Article

Rational Discovery of Antimicrobial Peptides by Means of Artificial Intelligence

期刊

MEMBRANES
卷 12, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/membranes12070708

关键词

antimicrobial; peptides; artificial intelligence; graphs; molecular dynamics

资金

  1. Colombian Ministry of Science, Technology, and Innovation (Minciencias) [120484467244]
  2. 2019 Fundacion Santafe de Bogota-Uniandes Grant: Production of recombinant antimicrobial peptides to modify materials of biomedical interest

向作者/读者索取更多资源

Antibiotic resistance is a global public health problem, and large pharmaceutical industries have stopped searching for new antibiotics due to low profitability. On the other hand, antimicrobial peptides (AMPs) have emerged as potent molecules with a lower rate of resistance. This study proposes using an artificial intelligence algorithm to improve the efficiency of high-activity AMP discovery.
Antibiotic resistance is a worldwide public health problem due to the costs and mortality rates it generates. However, the large pharmaceutical industries have stopped searching for new antibiotics because of their low profitability, given the rapid replacement rates imposed by the increasingly observed resistance acquired by microorganisms. Alternatively, antimicrobial peptides (AMPs) have emerged as potent molecules with a much lower rate of resistance generation. The discovery of these peptides is carried out through extensive in vitro screenings of either rational or non-rational libraries. These processes are tedious and expensive and generate only a few AMP candidates, most of which fail to show the required activity and physicochemical properties for practical applications. This work proposes implementing an artificial intelligence algorithm to reduce the required experimentation and increase the efficiency of high-activity AMP discovery. Our deep learning (DL) model, called AMPs-Net, outperforms the state-of-the-art method by 8.8% in average precision. Furthermore, it is highly accurate to predict the antibacterial and antiviral capacity of a large number of AMPs. Our search led to identifying two unreported antimicrobial motifs and two novel antimicrobial peptides related to them. Moreover, by coupling DL with molecular dynamics (MD) simulations, we were able to find a multifunctional peptide with promising therapeutic effects. Our work validates our previously proposed pipeline for a more efficient rational discovery of novel AMPs.

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