化学
抗菌剂
药品
抗菌药物
肽
计算生物学
抗感染药
抗药性
组合化学
药理学
微生物学
生物化学
生物
有机化学
作者
Yunxiang Yu,Zhang Zhou,Mengyun Gu,Wenjin Yan,Jian Han,Ruya Li,Lianhua Wei,Xin‐Lu Ren,Jinhui Tian,Shilin Xu,Rong Xia,Fu Y,Jinqi Huang
标识
DOI:10.1021/acs.jmedchem.5c00188
摘要
Antimicrobial resistance (AMR) presents a critical global health threat requiring urgent intervention. In order to swiftly respond to and control the spread of emerging drug-resistant bacteria at the onset of their proliferation, our aim is to develop a Rapid Response Antimicrobial Peptide (AMP) design strategy (RR-ADS). This framework addresses the challenge of limited pathogen-specific data by achieving robust generalization from minimal samples by meta-learning and reinforcement learning, optimizing both biocompatibility and efficacy against drug-resistant pathogens. Our model has achieved satisfactory results across multiple evaluation metrics, demonstrating the capability to accurately identify and generate AMPs targeted against drug-resistant bacteria with minimal sample sizes. Within 2 weeks, we successfully designed and experimentally verified AMPs against multidrug-resistant Acinetobacter baumannii, achieving a 93.3% positive rate. RR-ADS has effectively demonstrated the potential of meta-learning in tasks involving bioactive peptides and holds promise as an effective alternative measure to address infectious disease public health emergencies.
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