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10.3390/biom11030471

http://scihub22266oqcxt.onion/10.3390/biom11030471
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33810011!8004669!33810011
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suck abstract from ncbi

pmid33810011      Biomolecules 2021 ; 11 (3): ä
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  • Deep Learning for Novel Antimicrobial Peptide Design #MMPMID33810011
  • Wang C; Garlick S; Zloh M
  • Biomolecules 2021[Mar]; 11 (3): ä PMID33810011show ga
  • Antimicrobial resistance is an increasing issue in healthcare as the overuse of antibacterial agents rises during the COVID-19 pandemic. The need for new antibiotics is high, while the arsenal of available agents is decreasing, especially for the treatment of infections by Gram-negative bacteria like Escherichia coli. Antimicrobial peptides (AMPs) are offering a promising route for novel antibiotic development and deep learning techniques can be utilised for successful AMP design. In this study, a long short-term memory (LSTM) generative model and a bidirectional LSTM classification model were constructed to design short novel AMP sequences with potential antibacterial activity against E. coli. Two versions of the generative model and six versions of the classification model were trained and optimised using Bayesian hyperparameter optimisation. These models were used to generate sets of short novel sequences that were classified as antimicrobial or non-antimicrobial. The validation accuracies of the classification models were 81.6-88.9% and the novel AMPs were classified as antimicrobial with accuracies of 70.6-91.7%. Predicted three-dimensional conformations of selected short AMPs exhibited the alpha-helical structure with amphipathic surfaces. This demonstrates that LSTMs are effective tools for generating novel AMPs against targeted bacteria and could be utilised in the search for new antibiotics leads.
  • |*Deep Learning[MESH]
  • |Amino Acid Sequence[MESH]
  • |Area Under Curve[MESH]
  • |Bayes Theorem[MESH]
  • |Escherichia coli/*drug effects[MESH]
  • |Machine Learning[MESH]
  • |Molecular Conformation[MESH]
  • |Pore Forming Cytotoxic Proteins/*chemistry/pharmacology[MESH]
  • |Protein Conformation, alpha-Helical[MESH]


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