Sámano-Sánchez Hugo, Gibson Toby J
Structural and Computational Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany; Collaboration for Joint PhD Degree between EMBL and Heidelberg University, Faculty of Biosciences, 69120 Heidelberg, Germany.
Structural and Computational Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.
Trends Biochem Sci. 2020 Jun;45(6):526-544. doi: 10.1016/j.tibs.2020.03.003. Epub 2020 Mar 30.
Bacterial pathogens have developed complex strategies to successfully survive and proliferate within their hosts. Throughout the infection cycle, direct interaction with host cells occurs. Many bacteria have been found to secrete proteins, such as effectors and toxins, directly into the host cell with the potential to interfere with cell regulatory processes, either enzymatically or through protein-protein interactions (PPIs). Short linear motifs (SLiMs) are abundant peptide modules in cell signaling proteins. Here, we cover the reported examples of eukaryotic-like SLiM mimicry being used by pathogenic bacteria to hijack host cell machinery and discuss how drugs targeting SLiM-regulated cell signaling networks are being evaluated for interference with bacterial infections. This emerging anti-infective opportunity may become an essential contributor to antibiotic replacement strategies.
细菌病原体已形成复杂的策略,以便在宿主内成功存活和增殖。在整个感染周期中,都会发生与宿主细胞的直接相互作用。已发现许多细菌会将效应蛋白和毒素等蛋白质直接分泌到宿主细胞中,这些蛋白质有可能通过酶促作用或通过蛋白质-蛋白质相互作用(PPI)干扰细胞调节过程。短线性基序(SLiM)是细胞信号蛋白中丰富的肽模块。在这里,我们涵盖了已报道的致病细菌利用类似真核生物的SLiM模拟来劫持宿主细胞机制的例子,并讨论了针对SLiM调节的细胞信号网络的药物如何被评估用于干扰细菌感染。这种新出现的抗感染机会可能成为抗生素替代策略的重要贡献者。