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A designed RNA selection: establishment of a stable complex between a target and selectant RNA via two coordinated interactions.


ABSTRACT: In this paper, we describe a new method for selecting RNA aptamers that cooperatively bind to two specific sites within a target RNA. We designed a selection system in which two RNAs, a target RNA and a RNA pool, were assembled by employing a pre-organized GAAA tetraloop-11-nt receptor interaction. This allows us to select the binding sequence against a targeted internal loop as well as a linker region optimized for binding of the two binding sites. After the selection, the aptamers bound with dissociation constants in the nanomolar range, thereby forming a stable complex with the target RNA. Thus this method enables identification of aptamers for a specific binding site together with a linker for cooperative binding of the two RNAs. It appears that our new method can be applied generally to select RNAs that adhere tightly to a target RNA via two specific sites. The method can also be applicable for further engineering of both natural and artificial RNAs.

SUBMITTER: Shiohara T 

PROVIDER: S-EPMC2647284 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

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A designed RNA selection: establishment of a stable complex between a target and selectant RNA via two coordinated interactions.

Shiohara Tomoaki T   Saito Hirohide H   Inoue Tan T  

Nucleic acids research 20090109 3


In this paper, we describe a new method for selecting RNA aptamers that cooperatively bind to two specific sites within a target RNA. We designed a selection system in which two RNAs, a target RNA and a RNA pool, were assembled by employing a pre-organized GAAA tetraloop-11-nt receptor interaction. This allows us to select the binding sequence against a targeted internal loop as well as a linker region optimized for binding of the two binding sites. After the selection, the aptamers bound with d  ...[more]

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