AMP-BERT

AMP-BERT predicts antimicrobial peptide (AMP) function by fine-tuning a BERT (Bidirectional Encoder Representations from Transformers) model on peptide sequences to identify and classify AMPs.


Key Features:

  • Deep Learning Architecture: Employs a fine-tuned BERT model adapted for peptide sequences to capture sequence-contextual information relevant to AMP activity.
  • Predictive Accuracy: Demonstrates high predictive accuracy in AMP classification in comparative evaluations against other machine learning and deep learning models using a curated external dataset.
  • Interpretable Feature Analysis: Leverages BERT's attention mechanism to highlight specific residues and motifs that contribute to structural integrity and antimicrobial function.

Scientific Applications:

  • Drug Development: Identifies candidate AMPs to support discovery and validation of new antimicrobial agents.
  • Functional Validation: Pinpoints residues associated with antimicrobial activity to inform functional studies and peptide optimization.
  • Antimicrobial Resistance Research: Aids exploration of novel peptides as alternatives to conventional antibiotics and characterization of their roles in antimicrobial resistance.

Methodology:

Peptide sequences are input and preprocessed for compatibility with BERT; the BERT model is fine-tuned on a curated dataset of known AMPs and non-AMPs; following training, the model predicts AMP likelihood and uses its attention mechanism to analyze residues critical for antimicrobial function.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux
Programming Languages:
Python
Added:
2/9/2023
Last Updated:
11/24/2024

Operations

Publications

Lee H, Lee S, Lee I, Nam H. <scp>AMP‐BERT</scp>: Prediction of antimicrobial peptide function based on a <scp>BERT</scp> model. Protein Science. 2022;32(1). doi:10.1002/pro.4529. PMID:36461699. PMCID:PMC9793967.

PMID: 36461699
PMCID: PMC9793967
Funding: - Institute for Information and Communications Technology Promotion: 2019‐0‐01842 - National Research Foundation of Korea: NRF‐2020R1A2C2004628