2003•Humana Press eBooksRequires access

Design of Hairpin Ribozymes for In Vitro and Cellular Applications

Yu Qiao, John M. Burke

Open publisher page 15 citations

Abstract

Following the discovery of catalytic RNA ( 1 ), a number of different ribozymes have been found. Most ribozymes carry out site-specific cleavage of the RNA phosphodiester backbone, although important exceptions may be emerging ( 2 , 3 ). The catalytic center and reaction site of several naturally occurring self-cleaving molecules have been dissected, and used to develop ribozymes that cleave external substrates ( 4 ). Because RNA structure is responsible for both catalytic activity and substrate recognition, ribozymes may be engineered to direct the inactivation of targeted cellular and viral RNAs through a catalytic cleavage mechanism ( 5 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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What this paper is about

Following the discovery of catalytic RNA ( 1 ), a number of different ribozymes have been found. Most ribozymes carry out site-specific cleavage of the RNA phosphodiester backbone, although important exceptions may be emerging ( 2 , 3 ). The catalytic center and reaction site of several naturally occurring self-cleaving molecules have been dissected, and used to develop ribozymes that cleave external substrates ( 4 ). Because RNA structure is responsible for both catalytic activity and substrate recognition, ribozymes may be engineered to direct the inactivation of targeted cellular and viral RNAs through a catalytic cleavage mechanism ( 5 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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OpenAlex reports 15 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Following the discovery of catalytic RNA ( 1 ), a number of different ribozymes have been found. Most ribozymes carry out site-specific cleavage of the RNA phosphodiester backbone, although important exceptions may be emerging ( 2 , 3 ). The catalytic center and reaction site of several naturally occurring self-cleaving molecules have been dissected, and used to develop ribozymes that cleave external substrates ( 4 ). Because RNA structure is responsible for both catalytic activity and substrate recognition, ribozymes may be engineered to direct the inactivation of targeted cellular and viral RNAs through a catalytic cleavage mechanism ( 5 ). These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Key concepts: Ribozyme, Ligase ribozyme, Phosphodiester bond, Cleave, Cleavage (geology), RNA, Chemistry, In vitro

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