Evolutionary Dynamics and Functional Differences in Clinically Relevant Pen β-Lactamases from Burkholderia spp

Antimicrobial resistance (AMR) is a global threat, with species contributing significantly to difficult-to-treat infections. The Pen family of β-lactamases are produced by all spp., and their mutation or overproduction leads to the resistance of β-lactam antibiotics. Here we investigate the dynamic...

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Vydáno v:Journal of chemical information and modeling Ročník 65; číslo 10; s. 5086
Hlavní autoři: Gu, Jing, Agarwal, Pratul K, Bonomo, Robert A, Haider, Shozeb
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 26.05.2025
Témata:
beta-Lactamases - chemistry
beta-Lactamases - genetics
beta-Lactamases - metabolism
Burkholderia - enzymology
Catalytic Domain
Evolution, Molecular
Markov Chains
Molecular Dynamics Simulation
Mutation
ISSN:1549-960X, 1549-960X
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Shrnutí:Antimicrobial resistance (AMR) is a global threat, with species contributing significantly to difficult-to-treat infections. The Pen family of β-lactamases are produced by all spp., and their mutation or overproduction leads to the resistance of β-lactam antibiotics. Here we investigate the dynamic differences among four Pen β-lactamases (PenA, PenI, PenL and PenP) using machine learning driven enhanced sampling molecular dynamics simulations, Markov State Models (MSMs), convolutional variational autoencoder-based deep learning (CVAE) and the BindSiteS-CNN model. In spite of sharing the same catalytic mechanisms, these enzymes exhibit distinct dynamic features due to low sequence identity, resulting in different substrate profiles and catalytic turnover. The BindSiteS-CNN model further reveals local active site dynamics, offering insights into the Pen β-lactamase evolutionary adaptation. Our findings reported here identify critical mutations and propose new hot spots affecting Pen β-lactamase flexibility and function, which can be used to fight emerging resistance in these enzymes.
Bibliografie:ObjectType-Article-1
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ISSN:1549-960X
1549-960X
DOI:10.1021/acs.jcim.5c00271