Mathieu Sophie, Cissé Cheickna, Vitale Sylvia, Ahmadova Aynur, Degardin Mélissa, Pérard Julien, Colas Pierre, Miras Roger, Boturyn Didier, Covès Jacques, Crouzy Serge, Michaud-Soret Isabelle
CNRS, Laboratoire de Chimie et Biologie des Métaux (LCBM) UMR 5249 CNRS-CEA-UJF, F-38054 Grenoble, France.
CEA, LCBM, F-38054 Grenoble, France.
ACS Chem Biol. 2016 Sep 16;11(9):2519-28. doi: 10.1021/acschembio.6b00360. Epub 2016 Jul 19.
FUR (Ferric Uptake Regulator) protein is a global transcriptional regulator that senses iron status and controls the expression of genes involved in iron homeostasis, virulence, and oxidative stress. Ubiquitous in Gram-negative bacteria and absent in eukaryotes, FUR is an attractive antivirulence target since the inactivation of the fur gene in various pathogens attenuates their virulence. The characterization of 13-aa-long anti-FUR linear peptides derived from the variable part of the anti-FUR peptide aptamers, that were previously shown to decrease pathogenic E. coli strain virulence in a fly infection model, is described herein. Modeling, docking, and experimental approaches in vitro (activity and interaction assays, mutations) and in cells (yeast two-hybrid assays) were combined to characterize the interactions of the peptides with FUR, and to understand their mechanism of inhibition. As a result, reliable structure models of two peptide-FUR complexes are given. Inhibition sites are mapped in the groove between the two FUR subunits where DNA should also bind. Another peptide behaves differently and interferes with the dimerization itself. These results define these novel small peptide inhibitors as lead compounds for inhibition of the FUR transcription factor.
铁摄取调节蛋白(FUR)是一种全局转录调节因子,可感知铁状态并控制参与铁稳态、毒力和氧化应激的基因表达。FUR在革兰氏阴性菌中普遍存在,而在真核生物中不存在,由于各种病原体中fur基因的失活会减弱其毒力,因此FUR是一个有吸引力的抗毒力靶点。本文描述了从抗FUR肽适配体可变部分衍生的13个氨基酸长的抗FUR线性肽的特性,这些肽先前已在果蝇感染模型中显示出可降低致病性大肠杆菌菌株的毒力。结合体外(活性和相互作用测定、突变)和细胞内(酵母双杂交测定)的建模、对接和实验方法,以表征肽与FUR的相互作用,并了解其抑制机制。结果给出了两种肽-FUR复合物的可靠结构模型。抑制位点位于两个FUR亚基之间的凹槽中,DNA也应结合在此处。另一种肽表现不同,它会干扰二聚化本身。这些结果将这些新型小肽抑制剂定义为抑制FUR转录因子的先导化合物。