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Diff-AMP: tailored designed antimicrobial peptide framework with all-in-one generation, identification, prediction and optimization.

Authors :
Wang, Rui
Wang, Tao
Zhuo, Linlin
Wei, Jinhang
Fu, Xiangzheng
Zou, Quan
Yao, Xiaojun
Source :
Briefings in Bioinformatics. Mar2024, Vol. 25 Issue 2, p1-13. 13p.
Publication Year :
2024

Abstract

Antimicrobial peptides (AMPs), short peptides with diverse functions, effectively target and combat various organisms. The widespread misuse of chemical antibiotics has led to increasing microbial resistance. Due to their low drug resistance and toxicity, AMPs are considered promising substitutes for traditional antibiotics. While existing deep learning technology enhances AMP generation, it also presents certain challenges. Firstly, AMP generation overlooks the complex interdependencies among amino acids. Secondly, current models fail to integrate crucial tasks like screening, attribute prediction and iterative optimization. Consequently, we develop a integrated deep learning framework, Diff-AMP, that automates AMP generation, identification, attribute prediction and iterative optimization. We innovatively integrate kinetic diffusion and attention mechanisms into the reinforcement learning framework for efficient AMP generation. Additionally, our prediction module incorporates pre-training and transfer learning strategies for precise AMP identification and screening. We employ a convolutional neural network for multi-attribute prediction and a reinforcement learning-based iterative optimization strategy to produce diverse AMPs. This framework automates molecule generation, screening, attribute prediction and optimization, thereby advancing AMP research. We have also deployed Diff-AMP on a web server, with code, data and server details available in the Data Availability section. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14675463
Volume :
25
Issue :
2
Database :
Academic Search Index
Journal :
Briefings in Bioinformatics
Publication Type :
Academic Journal
Accession number :
176218869
Full Text :
https://doi.org/10.1093/bib/bbae078