SYNTHESIS AND ACTIVITY OF MODIFIED CYTIDINE 5′-MONOPHOSPHATE PROBES FOR T4 RNA LIGASE 1

被引:2
|
作者
Kore, Anilkumar R. [1 ]
Charles, Irudaya [1 ]
Yang, Litao [1 ]
Kuersten, Scott [1 ]
机构
[1] Life Technol Corp, Bioorgan Chem Div, Austin, TX 78744 USA
来源
关键词
T4 RNA ligase; pCp; p(5 ')C-4-biotin; A(5 ')pp(5 ')C-4-biotin; base modified cytidine; T4-RNA LIGASE; ACID LIGASE; OLIGODEOXYRIBONUCLEOTIDES; OLIGORIBONUCLEOTIDES; 3'; 5'-BISPHOSPHATES;
D O I
10.1080/15257770902946181
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
We describe the synthesis of a series of unique base modified ligation probes such as p(5')C-4-ethylenediamino 3, P(5')C-4-biotin 4, and pre-adenylated form A(5')pp(5')C-4-biotin 6 and tested. their biological activity with T4 RNA ligase I using a standard. pCp probe I as a control. The intermolecular ligation assay was developed, using a 5'-FAM labeled, 24 mer single-stranded (ss) RNA and the average ligation efficiencies for pCp 1, p(5')C-4-elhylenediamino 3, p(5')C4-biotin 4, and pre-adenylated form A(5')pp(5')C-4-biotin 6 were found to be 44%, 81%, 39% and 16% respectively, as deter-mined using a denaturing gel analysis. Furthermore, confirmation of the ligation activity of the biotinylated probes to the RNA substrate was confirmed. by streptavidin conjugation and analysis by nondenaturing gel electrophoresis. These results strongly suggest that the new probes are valid substrates for T4 RNA ligase I and therefore could be useful for developing a miRNA detection system that includes rapid isolation, efficient labeling and detection of miRNAs on sensitivity-enhanced microarrays.
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收藏
页码:292 / 302
页数:11
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