Department of Biological, Chemical and Pharmaceutical Sciences and Technologies, Università degli Studi di Palermo, Viale delle Scienze, 90128, Palermo, Italy.
Université de Lorraine and CNRS, LPCT UMR 7019, 54000, Nancy, France.
Chemistry. 2021 Jun 16;27(34):8865-8874. doi: 10.1002/chem.202100993. Epub 2021 May 13.
Human telomeric DNA, in G-quadruplex (G4) conformation, is characterized by a remarkable structural stability that confers it the capacity to resist to oxidative stress producing one or even clustered 8-oxoguanine (8oxoG) lesions. We present a combined experimental/computational investigation, by using circular dichroism in aqueous solutions, cellular immunofluorescence assays and molecular dynamics simulations, that identifies the crucial role of the stability of G4s to oxidative lesions, related also to their biological role as inhibitors of telomerase, an enzyme overexpressed in most cancers associated to oxidative stress.
人类端粒 DNA 在 G-四链体 (G4) 构象中具有显著的结构稳定性,使其能够抵抗产生一个甚至簇状 8-氧鸟嘌呤 (8oxoG) 损伤的氧化应激。我们通过使用水溶液圆二色性、细胞免疫荧光测定和分子动力学模拟进行了一项联合实验/计算研究,确定了 G4 对氧化损伤的稳定性的关键作用,这也与其作为端粒酶抑制剂的生物学作用相关,端粒酶是一种在大多数与氧化应激相关的癌症中过度表达的酶。