TY - JOUR
T1 - Trans-acting RNAs as molecular probes for monitoring time-dependent structural change of an RNA complex adapting two structures
AU - Maeda, Yuri
AU - Furuta, Hiroyuki
AU - Ikawa, Yoshiya
N1 - Funding Information:
This work is supported by Grants-in-Aids on Innovative Areas “Emergence in Chemistry” (No. 21111518 to Y.I.) and for the Global COE Program “Science for Future Molecular Systems” (H.F.) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan .
PY - 2011/3
Y1 - 2011/3
N2 - As dynamic structural changes are pivotal for the functions of some classes of RNA molecule, it is important to develop methods to monitor structural changes in RNA in a time-dependent manner without chemical modification. Based on previous reports that trans-acting RNAs can be used as probes for analysis and control of 3D structures of target RNAs, we applied this method to monitor time-dependent structural changes in RNA. We designed and performed a proof-of-principle study using a simple model RNA complex that adopts two different structures as a target. The time-dependent structural changes in the target RNA were successfully monitored using two trans-acting RNAs, which stably form a ternary complex with the bimolecular target RNA and act as a catalyst to join two RNA fragments of the target complex, respectively.
AB - As dynamic structural changes are pivotal for the functions of some classes of RNA molecule, it is important to develop methods to monitor structural changes in RNA in a time-dependent manner without chemical modification. Based on previous reports that trans-acting RNAs can be used as probes for analysis and control of 3D structures of target RNAs, we applied this method to monitor time-dependent structural changes in RNA. We designed and performed a proof-of-principle study using a simple model RNA complex that adopts two different structures as a target. The time-dependent structural changes in the target RNA were successfully monitored using two trans-acting RNAs, which stably form a ternary complex with the bimolecular target RNA and act as a catalyst to join two RNA fragments of the target complex, respectively.
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U2 - 10.1016/j.jbiosc.2010.11.007
DO - 10.1016/j.jbiosc.2010.11.007
M3 - Article
C2 - 21163698
AN - SCOPUS:79951811667
SN - 1389-1723
VL - 111
SP - 370
EP - 376
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 3
ER -