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理解噬菌体尾纤维与宿主表面受体的相互作用:重新编程噬菌体宿主范围的关键“蓝图”。

Understanding Bacteriophage Tail Fiber Interaction with Host Surface Receptor: The Key "Blueprint" for Reprogramming Phage Host Range.

机构信息

Bacteriophage Medical Research Center, Department of Biology, The Catholic University of America, Washington, DC 20064, USA.

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Int J Mol Sci. 2022 Oct 12;23(20):12146. doi: 10.3390/ijms232012146.

Abstract

Bacteriophages (phages), as natural antibacterial agents, are being rediscovered because of the growing threat of multi- and pan-drug-resistant bacterial pathogens globally. However, with an estimated 10 phages on the planet, finding the right phage to recognize a specific bacterial host is like looking for a needle in a trillion haystacks. The host range of a phage is primarily determined by phage tail fibers (or spikes), which initially mediate reversible and specific recognition and adsorption by susceptible bacteria. Recent significant advances at single-molecule and atomic levels have begun to unravel the structural organization of tail fibers and underlying mechanisms of phage-host interactions. Here, we discuss the molecular mechanisms and models of the tail fibers of the well-characterized T4 phage's interaction with host surface receptors. Structure-function knowledge of tail fibers will pave the way for reprogramming phage host range and will bring future benefits through more-effective phage therapy in medicine. Furthermore, the design strategies of tail fiber engineering are briefly summarized, including machine-learning-assisted engineering inspired by the increasingly enormous amount of phage genetic information.

摘要

噬菌体(phages)作为天然抗菌剂,由于全球多药和泛耐药细菌病原体的威胁日益增加,正在被重新发现。然而,据估计,地球上有 10 种噬菌体,要找到能够识别特定细菌宿主的正确噬菌体,就像在万亿干草堆中寻找一根针一样困难。噬菌体的宿主范围主要由噬菌体尾部纤维(或刺突)决定,这些纤维最初介导了可逆和特异性的识别和吸附作用,使易感细菌能够被噬菌体感染。最近在单分子和原子水平上的重大进展开始揭示尾部纤维的结构组织和噬菌体-宿主相互作用的潜在机制。在这里,我们讨论了 well-characterized T4 噬菌体与宿主表面受体相互作用的尾部纤维的分子机制和模型。了解尾部纤维的结构-功能关系将为噬菌体宿主范围的重新编程铺平道路,并通过在医学中更有效地使用噬菌体疗法带来未来的益处。此外,简要总结了尾部纤维工程的设计策略,包括受日益庞大的噬菌体遗传信息启发的机器学习辅助工程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b93/9603124/4db9eca29c59/ijms-23-12146-g001.jpg

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