Cryo-EM Reveals Structural Diversity in Prolate-headed Mycobacteriophage Mycofy1

IF 4.5 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2025-04-03 DOI:10.1016/j.jmb.2025.169126
Xiangyun Li , Qianqian Shao , Lin Li , Linlin Xie , Zhiyang Ruan , Qianglin Fang
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Abstract

Mycobacteriophages show promise in treating antibiotic-resistant mycobacterial infections. Here, we isolated Mycofy1, a mycobacteriophage, using M. smegmatis as a host. Cryo-EM analysis revealed that Mycofy1 possesses a prolate head and a long non-contractile tail. We determined structures of its head, head-to-tail interface, terminator, and tail tube to resolutions of ∼3.5 Å. Unexpectedly, we identified two distinct types of prolate head structures, exhibiting a 36° relative rotation in the top cap region. Additionally, the head-to-tail interface demonstrated flexibility. Our structures provide high-resolution cryo-EM data of a mycobacteriophage with a prolate head, as well as detailed structural information of the head-to-tail interface and head-proximal tail region in this phage group. These findings advance our understanding of assembly mechanisms in tailed bacteriophages.

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低温电镜显示长头分枝噬菌体Mycofy1的结构多样性。
噬分枝杆菌病毒有望治疗耐抗生素分枝杆菌感染。在这里,我们以M. smegmatis为宿主,分离出了一种噬分枝杆菌病毒Mycofy1。低温电子显微镜分析表明,Mycofy1 具有一个凸出的头部和一个非收缩的长尾。我们测定了其头部、头尾接口、终止子和尾管的结构,分辨率为 3.5 Å。此外,头部到尾部的界面也表现出灵活性。我们的结构首次提供了噬分枝杆菌噬菌体长头的高分辨率低温电子显微镜数据,并提供了该噬菌体组中头-尾界面和头-近尾区域的详细结构信息。这些发现增进了我们对有尾噬菌体组装机制的了解。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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