中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
G-Quadruplex binding enantiomers show chiral selective interactions with human telomere

文献类型:期刊论文

作者Wang, Jiasi ; Chen, Yong ; Ren, Jinsong ; Zhao,Chuanqi ; Qu,Xiaogang
刊名nucleic acids research
出版日期2014
卷号42期号:6页码:3792-3802
关键词END-PROTECTION PROBLEM DNA-DAMAGE RESPONSE REVERSE-TRANSCRIPTASE LIGAND RHPS4 CANCER-CELLS IN-VITRO NUCLEAR TRANSLOCATION ANTITUMOR-ACTIVITY LEUKEMIA-CELLS INHIBITION
ISSN号0305-1048
通讯作者qu,xg
中文摘要chiral recognition of dna molecules is important because dna chiral transition and its different conformations are involved in a series of important life events. among them, polymorphic human telomere dna has attracted great interests in recent years because of its important roles in chromosome structural integrity. in this report, we examine the short-term effect of chiral metallo-supramolecular complex enantiomers treatment on tumor cells, and find that a zinc-finger-like alpha helical chiral metallo-supramolecular complex, [ni2l3](4+)-p enantiomer (nip), can selectively provoke the rapid telomere uncapping, trigger dna damage responses at telomere and degradation of g-overhang and the delocalization of telomeric protein from telomeres. further studies indicate that nip can induce an acute cellular apoptosis and senescence in cancer cells rather than normal cells.
收录类别SCI收录期刊论文
语种英语
WOS记录号WOS:000334758600034
公开日期2015-03-25
源URL[http://ir.ciac.jl.cn/handle/322003/50661]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Wang, Jiasi,Chen, Yong,Ren, Jinsong,et al. G-Quadruplex binding enantiomers show chiral selective interactions with human telomere[J]. nucleic acids research,2014,42(6):3792-3802.
APA Wang, Jiasi,Chen, Yong,Ren, Jinsong,Zhao,Chuanqi,&Qu,Xiaogang.(2014).G-Quadruplex binding enantiomers show chiral selective interactions with human telomere.nucleic acids research,42(6),3792-3802.
MLA Wang, Jiasi,et al."G-Quadruplex binding enantiomers show chiral selective interactions with human telomere".nucleic acids research 42.6(2014):3792-3802.

入库方式: OAI收割

来源:长春应用化学研究所

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