磷光
细胞质
铱
核酸
化学
G-四倍体
共发射极
光化学
材料科学
DNA
光电子学
荧光
物理
生物化学
催化作用
光学
作者
Shaokang Jia,Wenjin Wang,Shanshan Qin,Shengjie Xie,Lisi Zhan,Qi Wei,Ziang Lu,Xiaolu Zhou,Cong Chen,Kun Chen,Shen Yan,Cai‐Ping Tan,Zong‐Wan Mao,Xiang Zhou
标识
DOI:10.1016/j.cclet.2022.05.031
摘要
G-quadruplex (G4) is widely known as a non-classical secondary structure of nucleic acid. With the in-depth study of G4, it is an urgent need for a phosphorescent probe with a high G4 binding ability to evaluate the level of G4 in the cytoplasm. Thus, this study designed and synthesized Ir-PDP where an Ir(III) complex was used as a phosphorescent emitter. Meanwhile, two installed PDPs (pyridostatin derivatives) were used to improve the combination ability with G4 and reduced the cytotoxicity of the Ir(III) complex. Compared with other nucleic acid secondary structures, Ir-PDP produced a higher phosphorescence lifetime after interacting with G4. Ir-PDP was distributed in the cytoplasm of living cells, and two-photon phosphorescence lifetime imaging can detect the binding events of the probe in the cytoplasm. The addition of G4 binder PDS significantly regulated cytoplasmic phosphorescence lifetime. The project explored a new sensing pathway to observe the binding manners of probes in the cytoplasm through the phosphorescence lifetime of probes. By installing the G4 ligand PDP on the iridium complex, we synthesized a phosphorescent probe that can label G4 in the cytoplasm, and the level of G4 in the cytoplasm can be explored through the phosphorescent lifetime of the probe.
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