Nanopore-Based Single-Molecule Investigation of Cation Effect on the i-Motif Structure

被引:1
|
作者
Wang, Zhenzhao [1 ]
Cui, Rikun [1 ]
Liu, Lili [1 ]
Li, Linna [1 ]
Li, Zhen [1 ]
Liu, Xingtong [1 ]
Guo, Yanli [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Xian 710127, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2024年 / 128卷 / 28期
基金
美国国家科学基金会;
关键词
G-QUADRUPLEX; DNA; PROTEIN;
D O I
10.1021/acs.jpcb.4c02021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The i-motif, a secondary structure of a four-helix formed by cytosine-rich DNA (i-DNA) through C-C+ base pairing, is prevalent in human telomeres and promoters. This structure creates steric hindrance, thereby inhibiting both gene expression and protein coding. The conformation of i-DNA is intricately linked to the intracellular ionic environment. Hence, investigating its conformation under various ion conditions holds significant importance. In this study, we explored the impact of cations on the i-motif structure at the single-molecule level using the alpha-hemolysin (alpha-HL) nanochannel. Our findings reveal that the ability of i-DNA to fold into the i-motif structure follows the order Cs+ > Na+ > K+ > Li+ for monovalent cations. Furthermore, we observed the interconversion of single-stranded DNA (ss-DNA) and the i-motif structure at high and low concentrations of Mg2+ and Ba2+ electrolyte solutions. This study not only has the potential to extend the application of i-motif-based sensors in complex solution environments but also provides a new idea for the detection of metal ions.
引用
收藏
页码:6830 / 6837
页数:8
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