Literature DB >> 10074465

A small catalytic RNA motif with Diels-Alderase activity.

B Seelig1, A Jäschke.   

Abstract

BACKGROUND: The 'RNA world' hypothesis requires that RNA be able to catalyze a wide variety of chemical reactions. In vitro selection from combinatorial RNA libraries has been used to identify several catalytic activities, most of which have resulted in a self-modification of RNA at one of its constituents. The formation of carbon-carbon bonds is considered an essential prerequisite for a complex metabolism based on RNA.
RESULTS: We describe the selection and characterization of new ribozymes that catalyze carbon-carbon bond formation by Diels-Alder reaction of a biotinylated maleimide with an RNA-tethered anthracene. Secondary structure analysis identified a 49-nucleotide RNA motif that accelerates the reaction about 20,000-fold. The motif has only 11 conserved nucleotides that are present in most of the selected sequences. The ribozyme motif is remarkably adaptable with respect to cofactor and metal-ion requirements. The motif was also re-engineered to give a 38-mer RNA that can act as a 'true' catalyst on short external substrate oligonucleotide-anthracene conjugates.
CONCLUSIONS: We have identified a small, highly abundant RNA motif that can solve the complex task of forming two carbon-carbon bonds between two reactants in trans, a catalytic capacity useful for creating prebiotically relevant molecules. This is the smallest and fastest RNA catalyst for carbon-carbon bond formation reported to date.

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Year:  1999        PMID: 10074465     DOI: 10.1016/S1074-5521(99)89008-5

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  65 in total

1.  Biochemistry. Reengineering enzymes.

Authors:  Stefan Lutz
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2.  Two independently selected capping ribozymes share similar substrate requirements.

Authors:  Hani S Zaher; R Ammon Watkins; Peter J Unrau
Journal:  RNA       Date:  2006-09-14       Impact factor: 4.942

3.  Structural basis for Diels-Alder ribozyme-catalyzed carbon-carbon bond formation.

Authors:  Alexander Serganov; Sonja Keiper; Lucy Malinina; Valentina Tereshko; Eugene Skripkin; Claudia Höbartner; Anna Polonskaia; Anh Tuân Phan; Richard Wombacher; Ronald Micura; Zbigniew Dauter; Andres Jäschke; Dinshaw J Patel
Journal:  Nat Struct Mol Biol       Date:  2005-02-20       Impact factor: 15.369

4.  Selection of ribozymes that catalyse multiple-turnover Diels-Alder cycloadditions by using in vitro compartmentalization.

Authors:  Jeremy J Agresti; Bernard T Kelly; Andres Jäschke; Andrew D Griffiths
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-31       Impact factor: 11.205

5.  Toward the selection of ribozymes for 1,3-dipolar cycloaddition reactions.

Authors:  Andreas Zerressen; Andres Jäschke
Journal:  J Mol Evol       Date:  2005-06-30       Impact factor: 2.395

6.  Recombination during in vitro evolution.

Authors:  Niles Lehman; Peter J Unrau
Journal:  J Mol Evol       Date:  2005-06-30       Impact factor: 2.395

7.  Control of stereoselectivity in an enzymatic reaction by backdoor access.

Authors:  Richard Wombacher; Sonja Keiper; Sandra Suhm; Alexander Serganov; Dinshaw J Patel; Andres Jäschke
Journal:  Angew Chem Int Ed Engl       Date:  2006-04-03       Impact factor: 15.336

Review 8.  Functional nucleic acid sensors.

Authors:  Juewen Liu; Zehui Cao; Yi Lu
Journal:  Chem Rev       Date:  2009-05       Impact factor: 60.622

Review 9.  In vitro selection using modified or unnatural nucleotides.

Authors:  Scott M Knudsen; Michael P Robertson; Andrew D Ellington
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2002-02

10.  Enhanced deoxyribozyme-catalyzed RNA ligation in the presence of organic cosolvents.

Authors:  Anit K Behera; Kelsey J Schlund; Allen J Mason; Kennedy O Alila; Mengyu Han; Rebecca L Grout; Dana A Baum
Journal:  Biopolymers       Date:  2013-06       Impact factor: 2.505

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