Cationic Porphyrin-Mediated G-Quadruplex DNA Oxidative Damage: Regulated by the Initial Interplay between DNA and TMPyP4

被引:5
|
作者
Zhou, Wenqin [1 ,2 ,3 ]
Cheng, Yu [2 ]
Song, Bo [4 ]
Hao, Jingya [2 ]
Miao, Wenhui [2 ,3 ]
Jia, Guoqing [2 ]
Li, Can [1 ,2 ]
机构
[1] Dalian Univ Technol, Zhang Dayu Sch Chem, Dalian 116024, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
GENE; PHOTOCLEAVAGE; GENERATION; RNA;
D O I
10.1021/acs.biochem.1c00557
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G-quadruplex (G4) ligand-induced DNA damage has been involved in many physiological functions of cells. Herein, cationic porphyrin (TMPyP4)-mediated DNA oxidation damage was investigated aiming at mitochondrial G4 DNA (mt9438) and its structural analogue of the thrombin-binding aptamer (TBA). TMPyP4 is found to stabilize TBA G4 but destabilize mt9438. For two resulting DNA-TMPyP4 assemblies, the distinct light-induced singlet oxygen (O-1(2)) generation and the subsequent DNA damage were found. For mt9438-TMPyP4, a slower O-1(2)-induced DNA damage takes place and results in the formation of DNA aggregation. In contrast, O-1(2) tends to promote DNA unfolding in a relatively faster rate for TBA-TMPyP4. Despite of such distinct DNA damage behavior, UV resonance Raman spectra reveal that for both mt9438-TMPyP4 and TBA-TMPyP4 the DNA damage commonly stems from the guanine-specific oxidation. Our results clearly indicate that the ligand-mediated DNA damage is strongly dependent on the initial interplay between DNA and the ligand.
引用
收藏
页码:3707 / 3713
页数:7
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