Your browser doesn't support javascript.
loading
Dynamic Structures and Fast Transition Kinetics of Oxidized G-Quadruplexes.
Ji, Jiahao; Sharma, Arpit; Pokhrel, Pravin; Karna, Deepak; Pandey, Shankar; Zheng, Yao-Rong; Mao, Hanbin.
Afiliação
  • Ji J; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Sharma A; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Pokhrel P; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Karna D; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Pandey S; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Zheng YR; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
  • Mao H; Department of Chemistry & Biochemistry, Kent State University, Kent, OH, 44242, USA.
Small ; : e2400485, 2024 Apr 28.
Article em En | MEDLINE | ID: mdl-38678502
ABSTRACT
8-oxoguanines (8-oxoG) in cells form compromised G-quadruplexes (GQs), which may vary GQ mediated gene regulations. By mimicking molecularly crowded cellular environment using 40% DMSO or sucrose, here it is found that oxidized human telomeric GQs have stabilities close to the wild-type (WT) GQs. Surprisingly, while WT GQs show negative formation cooperativity between a Pt(II) binder and molecularly crowded environment, positive cooperativity is observed for oxidized GQ formation. Single-molecule mechanical unfolding reveals that 8-oxoG sequence formed more diverse and flexible structures with faster folding/unfolding transition kinetics, which facilitates the Pt(II) ligand to bind the best-fit structures with positive cooperativity. These findings offer new understanding on structures and properties of oxidized G-rich species in crowded environments. They also provide insights into the design of better ligands to target oxidized G-rich structures formed under oxidative cell stress.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Small Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Small Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos