Novel RNA catalysts for the Michael reaction

被引:89
作者
Sengle, G
Eisenführ, A
Arora, PS
Nowick, JS
Famulok, M
机构
[1] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
来源
CHEMISTRY & BIOLOGY | 2001年 / 8卷 / 05期
关键词
Michael-addition; in vitro selection; RNA catalysis; ribozyme; RNA world;
D O I
10.1016/S1074-5521(01)00026-6
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
Background: In vitro selected ribozymes with nucleotide synthase, peptide and carbon-carbon bond forming activity provide insight into possible scenarios on how chemical transformations mag. have been catalyzed before protein enzymes had evolved. Metabolic pathways based on ribozymes may have existed at an early stage of evolution. Results: We have isolated a novel ribozyme that mediates Michael-adduct formation at a Michael-acceptor substrate, similar to the rate-limiting step of the mechanistic sequence of thymidylate synthase. The kinetic characterization of this catalyst revealed a rate enhancement by a factor of similar to 10(5). The ribozyme shows substrate specificity and can act as an intermolecular catalyst which transfers the Michael-donor substrate onto an external 20-mer RNA oligonucleotide containing the Michael-acceptor system. Conclusions: The ribozyme described here is the first example of a catalytic RNA with Michael-adduct forming activity which represents a key mechanistic step in metabolic pathways and other biochemical reactions. Therefore, previously unforeseen RNA-evolution pathways can be considered, for example the formation of dTMP from dUMP. The substrate specificity of this ribozyme may also render it useful in organic syntheses. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:459 / 473
页数:15
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