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革兰氏阴性菌表面脂蛋白:恶劣环境中的保护者和觅食者。

The surface lipoproteins of gram-negative bacteria: Protectors and foragers in harsh environments.

机构信息

Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada.

Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada.

出版信息

J Biol Chem. 2021 Jan-Jun;296:100147. doi: 10.1074/jbc.REV120.008745. Epub 2020 Dec 10.

Abstract

Gram-negative pathogens are enveloped by an outer membrane that serves as a double-edged sword: On the one hand, it provides a layer of protection for the bacterium from environmental insults, including other bacteria and the host immune system. On the other hand, it restricts movement of vital nutrients into the cell and provides a plethora of antigens that can be detected by host immune systems. One strategy used to overcome these limitations is the decoration of the outer surface of gram-negative bacteria with proteins tethered to the outer membrane through a lipid anchor. These surface lipoproteins (SLPs) fulfill critical roles in immune evasion and nutrient acquisition, but as more bacterial genomes are sequenced, we are beginning to discover their prevalence and their different roles and mechanisms and importantly how we can exploit them as antimicrobial targets. This review will focus on representative SLPs that gram-negative bacteria use to overcome host innate immunity, specifically the areas of nutritional immunity and complement system evasion. We elaborate on the structures of some notable SLPs required for binding target molecules in hosts and how this information can be used alongside bioinformatics to understand mechanisms of binding and in the discovery of new SLPs. This information provides a foundation for the development of therapeutics and the design of vaccine antigens.

摘要

革兰氏阴性病原体被一层外膜包裹,这层外膜可谓一把双刃剑:一方面,它为细菌提供了一层保护,使其免受环境侵害,包括其他细菌和宿主免疫系统的侵害。另一方面,它限制了重要营养物质进入细胞的运动,并提供了大量宿主免疫系统可以检测到的抗原。克服这些限制的一种策略是通过脂质锚将与外膜相连的蛋白质修饰在革兰氏阴性菌的外表面。这些表面脂蛋白 (SLP) 在免疫逃避和营养获取中发挥着关键作用,但随着越来越多的细菌基因组被测序,我们开始发现它们的普遍性以及它们不同的作用机制,重要的是,我们可以如何将它们作为抗菌靶点加以利用。本综述将重点介绍革兰氏阴性菌用于克服宿主先天免疫的代表性 SLP,特别是营养免疫和补体系统逃避的领域。我们详细阐述了一些值得注意的 SLP 的结构,这些 SLP 用于与宿主中的靶分子结合,以及如何将这些信息与生物信息学结合使用,以了解结合机制,并发现新的 SLP。这些信息为治疗药物的开发和疫苗抗原的设计提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4051/7857515/556b11675a10/gr1.jpg

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