Department of Microbial Sciences, Institute of Biology, Leiden University, Sylviusweg 72, 2333 BE Leiden, the Netherlands; MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, School of Physics, Xi'an Jiaotong University, Xianning West Road 28, Xi'an 710049, China.
Department of Microbial Sciences, Institute of Biology, Leiden University, Sylviusweg 72, 2333 BE Leiden, the Netherlands; Centre for Microbial Cell Biology, Leiden University, Leiden, the Netherlands.
Curr Opin Microbiol. 2024 Feb;77:102429. doi: 10.1016/j.mib.2024.102429. Epub 2024 Jan 26.
Bacteriophages are being rediscovered as potent agents for medical and industrial applications. However, finding a suitable phage relies on numerous factors, including host specificity, burst size, and infection cycle. The host range of a phage is, besides phage defense systems, initially determined by the recognition and attachment of receptor-binding proteins (RBPs) to the target receptors of susceptible bacteria. RBPs include tail (or occasionally head) fibers and tailspikes. Owing to the potential flexibility and heterogeneity of these structures, they are often overlooked during structural studies. Recent advances in cryo-electron microscopy studies and computational approaches have begun to unravel their structural and fundamental mechanisms during phage infection. In this review, we discuss the current state of research on different phage tail and head fibers, spike models, and molecular mechanisms. These details may facilitate the manipulation of phage-host specificity, which in turn will have important implications for science and society.
噬菌体正作为医学和工业应用的有效试剂重新被发现。然而,寻找合适的噬菌体依赖于许多因素,包括宿主特异性、爆发大小和感染周期。噬菌体的宿主范围除了噬菌体防御系统外,最初还取决于受体结合蛋白 (RBP) 对易感细菌靶受体的识别和附着。RBP 包括尾部 (或偶尔头部) 纤维和尾部刺突。由于这些结构具有潜在的灵活性和异质性,它们在结构研究中经常被忽视。最近在低温电子显微镜研究和计算方法方面的进展,开始揭示了噬菌体感染过程中它们的结构和基本机制。在这篇综述中,我们讨论了不同噬菌体尾部和头部纤维、刺突模型以及分子机制的研究现状。这些细节可能有助于操纵噬菌体-宿主特异性,这反过来又将对科学和社会产生重要影响。