Ambite Ines, Wan Murphy Lam Yim, Tran Hien Thi, Nazari Atefeh, Chaudhuri Arunima, Krintel Christian, Gomes Inês, Sabari Samudra, Ahmadi Shahram, Carneiro António N B M, Ishac Rita, Haq Farhan, Svanborg Catharina
Department of Laboratory Medicine, Division of Microbiology, Immunology and Glycobiology, Lund University, Klinikgatan 28, Lund, 221 84, Sweden.
Sci Rep. 2025 Feb 25;15(1):6778. doi: 10.1038/s41598-025-88093-2.
Identifying specific inhibitors of the MYC oncogene has been challenging, due to off target effects associated with MYC inhibition. This study investigated how the recombinant Escherichia coli Lon protease (rLon), which targets MYC in human cells, inhibits MYC over-activation in models of infection and cancer. In silico predictions identified specific peptide domains of bacterial Lon that target MYC and the affinity of these peptides for MYC was investigated by surface plasmon resonance. The N-terminal domain of rLon was shown to interact with the C-terminal, leucine zipper domain of MYC and MAX and to prevent MYC/MAX dimerization. Furthermore, rLon targeted and degraded c-MYC in vitro and in cellular models, through the peptidase domain. In a model of kidney infection, rLon treatment prevented, c-MYC, N-MYC and L-MYC over-expression, MYC-dependent gene expression, specifically renal toxicity genes and pathology, suggesting that rLon recognizes and corrects MYC dysregulation in this disease. The findings describe a multitarget mechanism of MYC inhibition by rLon, and the combined effects achieved by the Lon domains, targeting different MYC epitopes and MYC-dependent functions, with no evidence of toxicity or detrimental effects on homeostatic MYC expression.
由于与MYC抑制相关的脱靶效应,鉴定MYC癌基因的特异性抑制剂一直具有挑战性。本研究调查了在人类细胞中靶向MYC的重组大肠杆菌Lon蛋白酶(rLon)如何在感染和癌症模型中抑制MYC的过度激活。计算机预测确定了细菌Lon靶向MYC的特定肽结构域,并通过表面等离子体共振研究了这些肽对MYC的亲和力。结果表明,rLon的N端结构域与MYC和MAX的C端亮氨酸拉链结构域相互作用,并阻止MYC/MAX二聚化。此外,rLon通过肽酶结构域在体外和细胞模型中靶向并降解c-MYC。在肾脏感染模型中,rLon治疗可预防c-MYC、N-MYC和L-MYC的过表达、MYC依赖性基因表达,特别是肾毒性基因和病理变化,这表明rLon在该疾病中识别并纠正了MYC的失调。这些发现描述了rLon抑制MYC的多靶点机制,以及Lon结构域通过靶向不同的MYC表位和MYC依赖性功能所产生的联合效应,且没有对稳态MYC表达产生毒性或有害影响的证据。