Structure of an F-type phage tail-like bacteriocin from Listeria monocytogenes

F-type phage tail-like bacteriocins (PTLBs) are high-molecular-weight protein complexes exhibiting bactericidal activity and share evolutionary similarities with the tails of non-contractile siphoviruses. In this study, we present the atomic structure of monocin, a genetically engineered F-type PTLB from Listeria monocytogenes. Our detailed atomic-level analysis, excluding two chaperone proteins, provides crucial insights into the molecular architecture of F-type PTLBs. The core structure of monocin resembles TP901-1-like phage tails, featuring three side fibers with receptor-binding domains that connect to the baseplate for host adhesion. Based on these findings, we propose a potential mechanism by which F-type PTLBs induce cell death, offering a foundation for developing targeted antibacterial therapies.

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Publication Details

Journal
Nature Communications
Published
2025-02-16
DOI
https://doi.org/10.1038/s41467-025-57075-3
Citations
3
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
5.15

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article

Structure of an F-type phage tail-like bacteriocin from Listeria monocytogenes

Xiaofei Ge, Jiawei Wang, Zhiwei Gu
3 citations
Nature Communications
Bacteriophages and microbial interactions
5.15
article

Structure of an F-type phage tail-like bacteriocin from Listeria monocytogenes

Xiaofei Ge, Jiawei Wang, Zhiwei Gu
article en
3 citations

Abstract

F-type phage tail-like bacteriocins (PTLBs) are high-molecular-weight protein complexes exhibiting bactericidal activity and share evolutionary similarities with the tails of non-contractile siphoviruses. In this study, we present the atomic structure of monocin, a genetically engineered F-type PTLB from Listeria monocytogenes. Our detailed atomic-level analysis, excluding two chaperone proteins, provides crucial insights into the molecular architecture of F-type PTLBs. The core structure of monocin resembles TP901-1-like phage tails, featuring three side fibers with receptor-binding domains that connect to the baseplate for host adhesion. Based on these findings, we propose a potential mechanism by which F-type PTLBs induce cell death, offering a foundation for developing targeted antibacterial therapies.

Nature CommunicationsVol. 16(1)
University of Macau (MO), Center for Life Sciences (CN), City University of Macau (MO), Tsinghua University (CN)
National Natural Science Foundation of China, Tsinghua University
Openalex Percentile: Top 6%
Bacteriophages and microbial interactions
5.15
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