A new selective 'turn-on' small fluorescent cationic probe for recognition of RNA in cells

被引:9
|
作者
Ahmed, Nisar [1 ]
Shirinfar, Bahareh [1 ]
Miriyala, Vijay Madhav [2 ,3 ]
Choi, Seong-Kyoon [4 ]
Lee, Kyeong-Min [4 ]
Jeon, Won Bae [4 ]
Park, Yu Shin [5 ]
Nam, Hong Gil [6 ,7 ]
机构
[1] Univ Zurich UZH, Dept Chem, CH-8057 Zurich, Switzerland
[2] Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, South Korea
[3] Univ Johannesburg, Dept Chem, ZA-2006 Johannesburg, South Africa
[4] Daegu Gyeongbuk Inst Sci & Technol, Div NanoBio Technol, Lab Biochem & Cellular Engn, Daegu 711873, South Korea
[5] DGIST, Ctr Core Res Facil, Daegu 711873, South Korea
[6] Inst Basic Sci IBS, Ctr Plant Aging Res, Daegu 711873, South Korea
[7] DGIST, Dept New Biol, Daegu 711873, South Korea
关键词
confocal microscopy; cationic probe; RNA recognition; host-guest chemistry; GENE-EXPRESSION; GUEST-HOST; IMIDAZOLIUM; RECEPTORS; ABUNDANCE; PROTEIN; PYRENE;
D O I
10.1080/10610278.2014.989851
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorescent imaging probes have revolutionised cell biology by monitoring cellular objects. However, the lack of fluorescent probes with high selectivity for RNA has been a drawback. Thus, selective RNA binding for fluorescent sensors is essential. Here, we report the selective fluorescence enhancement upon addition of RNA. By exploiting a selective recognition of small tetra-cationic probe 1 for RNA, we also explain the possible binding mode for RNA. As a membrane-permeant fluorescence probe, 1 provides selective imaging of RNA not only in human neuroblastoma tumour SH-SY5Y cell line used for Parkinson's disease but also in the unicellular green alga cells. Further exploitation could open new opportunities in neurotoxin and cancer biology.
引用
收藏
页码:478 / 483
页数:6
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