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敌友难辨:DNA促旋酶的蛋白质抑制剂

Friend or Foe: Protein Inhibitors of DNA Gyrase.

作者信息

Ruan Shengfeng, Tu Chih-Han, Bourne Christina R

机构信息

Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019, USA.

出版信息

Biology (Basel). 2024 Jan 29;13(2):84. doi: 10.3390/biology13020084.

Abstract

DNA gyrase is essential for the successful replication of circular chromosomes, such as those found in most bacterial species, by relieving topological stressors associated with unwinding the double-stranded genetic material. This critical central role makes gyrase a valued target for antibacterial approaches, as exemplified by the highly successful fluoroquinolone class of antibiotics. It is reasonable that the activity of gyrase could be intrinsically regulated within cells, thereby helping to coordinate DNA replication with doubling times. Numerous proteins have been identified to exert inhibitory effects on DNA gyrase, although at lower doses, it can appear readily reversible and therefore may have regulatory value. Some of these, such as the small protein toxins found in plasmid-borne addiction modules, can promote cell death by inducing damage to DNA, resulting in an analogous outcome as quinolone antibiotics. Others, however, appear to transiently impact gyrase in a readily reversible and non-damaging mechanism, such as the plasmid-derived Qnr family of DNA-mimetic proteins. The current review examines the origins and known activities of protein inhibitors of gyrase and highlights opportunities to further exert control over bacterial growth by targeting this validated antibacterial target with novel molecular mechanisms. Furthermore, we are gaining new insights into fundamental regulatory strategies of gyrase that may prove important for understanding diverse growth strategies among different bacteria.

摘要

DNA促旋酶对于环状染色体的成功复制至关重要,例如在大多数细菌物种中发现的环状染色体,它通过缓解与解开双链遗传物质相关的拓扑压力来实现这一功能。这种关键的核心作用使促旋酶成为抗菌方法的重要靶点,如极为成功的氟喹诺酮类抗生素就证明了这一点。促旋酶的活性在细胞内可能受到内在调节,从而有助于将DNA复制与倍增时间协调起来,这是合理的。尽管许多蛋白质已被鉴定出对DNA促旋酶有抑制作用,但在较低剂量下,这种抑制作用似乎很容易逆转,因此可能具有调节价值。其中一些蛋白质,如在质粒携带的成瘾模块中发现的小蛋白质毒素,可通过诱导DNA损伤来促进细胞死亡,其结果与喹诺酮类抗生素类似。然而,其他一些蛋白质似乎以一种易于逆转且无损伤的机制短暂影响促旋酶,例如质粒衍生的模拟DNA的Qnr蛋白家族。本综述探讨了促旋酶蛋白质抑制剂的起源和已知活性,并强调了通过利用新的分子机制靶向这一经过验证的抗菌靶点来进一步控制细菌生长的机会。此外,我们正在对促旋酶的基本调节策略获得新的见解,这可能对理解不同细菌之间的多种生长策略很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9013/10886550/d4a2b9ca5e94/biology-13-00084-g002.jpg

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