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Examination of specific binding activity of aptamer RNAs to the HIV-NC by using a cell-based in vivo assay for protein-RNA interaction
被引:9
|作者:
Jeong, Yu Young
[1
]
Kim, Seon Hee
[1
]
Jang, Soo In
[1
]
You, Ji Chang
[1
]
机构:
[1] Catholic Univ, Natl Res Lab Mol Virol, Dept Pathol, Coll Med, Seoul 137701, South Korea
来源:
关键词:
cell-based assay;
HIV nucleocapsid protein;
Protein-RNA interaction;
Psi (psi);
RNA aptamer;
D O I:
10.5483/BMBRep.2008.41.7.511
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:
The nucleocapsid (NQ protein of the Human Immunodeficiency Virus-1 plays a key role in viral genomic packaging by specifically recognizing the Psi(T) RNA sequence within the HIV-1 genome RNA. Recently, a novel cell-based assay was developed to probe the specific interactions in vivc) between the NC and T-RNA using Ecoli cells (I. WroL 81: 6151-55, 2007). In order to examine the extenclibility of this cell-based assay to RNAs other than T-RNA, this study tested the RNA aptamers isolated in vitro using the SELEX method, but whose specific binding ability to NC in a living cellular environment has not been established. The results demonstrate for the first time that each of those aptamer RNAs can bind specifically to NC in a NC zinc finger motif dependent manner within the cell. This confirms that the cell-based assay developed for NC-T interaction can be further extended and applied to NC-binding RNAs other than T-RNA.
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页码:511 / 515
页数:5
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