Resolving altered base-pairing of RNA modifications with DNA nanoswitches

被引:2
|
作者
Todkari, Iranna Annappa [1 ,2 ]
Chandrasekaran, Arun Richard [1 ]
Punnoose, Jibin Abraham [1 ]
Mao, Song [1 ,2 ]
Haruehanroengra, Phensinee [1 ,2 ]
Beckles, Camryn [1 ,2 ]
Sheng, Jia [1 ,2 ]
Halvorsen, Ken [1 ]
机构
[1] SUNY Albany, RNA Inst, Albany, NY 12222 USA
[2] SUNY Albany, Dept Chem, Albany, NY 12222 USA
关键词
FUNCTIONAL INSIGHTS; LANDSCAPE;
D O I
10.1093/nar/gkad802
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
There are >170 naturally occurring RNA chemical modifications, with both known and unknown biological functions. Analytical methods for detecting chemical modifications and for analyzing their effects are relatively limited and have had difficulty keeping pace with the demand for RNA chemical biology and biochemistry research. Some modifications can affect the ability of RNA to hybridize with its complementary sequence or change the selectivity of base pairing. Here, we investigate the use of affinity-based DNA nanoswitches to resolve energetic differences in hybridization. We found that a single m(3)C modification can sufficiently destabilize hybridization to abolish a detection signal, while an s4U modification can selectively hybridize with G over A. These results establish proof of concept for using DNA nanoswitches to detect certain RNA modifications and analyzing their effects in base pairing stability and specificity.
引用
收藏
页码:11291 / 11297
页数:7
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