Architecture et Fonction des Macromolécules Biologiques, Centre National de la Recherche Scientifique (CNRS), Campus de Luminy, Case 932, 13288 Marseille Cedex 09, France.
Architecture et Fonction des Macromolécules Biologiques, Aix-Marseille Université, Campus de Luminy, Case 932, 13288 Marseille Cedex 09, France.
Biochem Soc Trans. 2020 Apr 29;48(2):507-516. doi: 10.1042/BST20190638.
Bacteriophages (phages) and their preys are engaged in an evolutionary arms race driving the co-adaptation of their attack and defense mechanisms. In this context, phages have evolved diverse anti-CRISPR proteins to evade the bacterial CRISPR-Cas immune system, and propagate. Anti-CRISPR proteins do not share much resemblance with each other and with proteins of known function, which raises intriguing questions particularly relating to their modes of action. In recent years, there have been many structure-function studies shedding light on different CRISPR-Cas inhibition strategies. As the anti-CRISPR field of research is rapidly growing, it is opportune to review the current knowledge on these proteins, with particular emphasis on the molecular strategies deployed to inactivate distinct steps of CRISPR-Cas immunity. Anti-CRISPR proteins can be orthosteric or allosteric inhibitors of CRISPR-Cas machineries, as well as enzymes that irreversibly modify CRISPR-Cas components. This repertoire of CRISPR-Cas inhibition mechanisms will likely expand in the future, providing fundamental knowledge on phage-bacteria interactions and offering great perspectives for the development of biotechnological tools to fine-tune CRISPR-Cas-based gene edition.
噬菌体(phages)与其猎物之间存在着一场进化军备竞赛,推动了它们攻击和防御机制的共同适应。在这种情况下,噬菌体进化出了多种抗 CRISPR 蛋白来逃避细菌的 CRISPR-Cas 免疫系统并进行繁殖。抗 CRISPR 蛋白彼此之间以及与已知功能的蛋白之间没有太多相似之处,这引发了人们的兴趣,尤其是关于它们的作用模式。近年来,有许多结构-功能研究揭示了不同的 CRISPR-Cas 抑制策略。随着抗 CRISPR 研究领域的快速发展,现在正是审查这些蛋白质的现有知识的好时机,特别强调用于使 CRISPR-Cas 免疫的不同步骤失活的分子策略。抗 CRISPR 蛋白可以是 CRISPR-Cas 机器的正构或别构抑制剂,以及不可逆修饰 CRISPR-Cas 成分的酶。这种 CRISPR-Cas 抑制机制的组合可能会在未来扩大,为噬菌体-细菌相互作用提供基础知识,并为开发生物技术工具以微调基于 CRISPR-Cas 的基因编辑提供广阔的前景。