Literature DB >> 11983335

Rescue of an abasic hairpin ribozyme by cationic nucleobases: evidence for a novel mechanism of RNA catalysis.

Lori L Lebruska1, Iaroslav I Kuzmine, Martha J Fedor.   

Abstract

The hairpin ribozyme catalyzes a reversible phosphodiester cleavage reaction. We examined the roles of conserved nucleobases in catalysis using an abasic ribozyme rescue strategy. Loss of the active site G8 nucleobase reduced the cleavage rate constant by 350-fold while loss of A9 and A10 nucleobases reduced activity less than 10-fold. Certain heterocyclic amines restored partial activity when provided in solution to the variant lacking G8. Heterocyclic amines that were capable of rescue shared the exocyclic amine and cyclic amide in common with the Watson-Crick hydrogen bonding face of guanine. In contrast to the shallow pH dependence of unmodified ribozyme activity, rescue activity increased sharply with decreasing pH. These results support a novel model for RNA catalysis in which a cationic nucleobase contributes electrostatic stabilization to negative charge developing in the transition state.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11983335     DOI: 10.1016/s1074-5521(02)00130-8

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


  25 in total

1.  Single-molecule enzymology of RNA: essential functional groups impact catalysis from a distance.

Authors:  David Rueda; Gregory Bokinsky; Maria M Rhodes; Michael J Rust; Xiaowei Zhuang; Nils G Walter
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-24       Impact factor: 11.205

2.  Extensive molecular dynamics simulations showing that canonical G8 and protonated A38H+ forms are most consistent with crystal structures of hairpin ribozyme.

Authors:  Vojtech Mlýnský; Pavel Banás; Daniel Hollas; Kamila Réblová; Nils G Walter; Jirí Sponer; Michal Otyepka
Journal:  J Phys Chem B       Date:  2010-05-20       Impact factor: 2.991

3.  Structural basis for the fast self-cleavage reaction catalyzed by the twister ribozyme.

Authors:  Daniel Eiler; Jimin Wang; Thomas A Steitz
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-25       Impact factor: 11.205

4.  Chemical rescue, multiple ionizable groups, and general acid-base catalysis in the HDV genomic ribozyme.

Authors:  Anne T Perrotta; Timothy S Wadkins; Michael D Been
Journal:  RNA       Date:  2006-05-11       Impact factor: 4.942

5.  Self-association of adenine-dependent hairpin ribozymes.

Authors:  Yan-Li Li; Marie-Christine Maurel; Christine Ebel; Jacques Vergne; Vitaliy Pipich; Giuseppe Zaccai
Journal:  Eur Biophys J       Date:  2007-09-25       Impact factor: 1.733

6.  Quantum mechanical/molecular mechanical simulation study of the mechanism of hairpin ribozyme catalysis.

Authors:  Kwangho Nam; Jiali Gao; Darrin M York
Journal:  J Am Chem Soc       Date:  2008-03-18       Impact factor: 15.419

7.  A comparison of vanadate to a 2'-5' linkage at the active site of a small ribozyme suggests a role for water in transition-state stabilization.

Authors:  Andrew T Torelli; Jolanta Krucinska; Joseph E Wedekind
Journal:  RNA       Date:  2007-05-08       Impact factor: 4.942

8.  QM/MM studies of hairpin ribozyme self-cleavage suggest the feasibility of multiple competing reaction mechanisms.

Authors:  Vojtěch Mlýnský; Pavel Banáš; Nils G Walter; Jiří Šponer; Michal Otyepka
Journal:  J Phys Chem B       Date:  2011-11-08       Impact factor: 2.991

9.  Water in the active site of an all-RNA hairpin ribozyme and effects of Gua8 base variants on the geometry of phosphoryl transfer.

Authors:  Jason Salter; Jolanta Krucinska; Shabnam Alam; Valerie Grum-Tokars; Joseph E Wedekind
Journal:  Biochemistry       Date:  2006-01-24       Impact factor: 3.162

10.  Fluorescent N2,N3-epsilon-adenine nucleoside and nucleotide probes: synthesis, spectroscopic properties, and biochemical evaluation.

Authors:  Einat Sharon; Sébastien A Lévesque; Mercedes N Munkonda; Jean Sévigny; Denise Ecke; Georg Reiser; Bilha Fischer
Journal:  Chembiochem       Date:  2006-09       Impact factor: 3.164

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.