Literature DB >> 15364565

Reduced contact order and RNA folding rates.

T R Sosnick1, T Pan.   

Abstract

We investigated the relationship between RNA structure and folding rates accounting for hierarchical structural formation. Folding rates of two-state folding proteins correlate well with relative contact order, a quantitative measure of the number and sequence distance between tertiary contacts. These proteins do not form stable structures prior to the rate-limiting step. In contrast, most secondary structures are stably formed prior to the rate-limiting step in RNA folding. Accordingly, we introduce "reduced contact order", a metric that reflects only the number of residues available to participate in the conformational search after the formation of secondary structure. Plotting the folding rates and the reduced contact order from ten different RNAs suggests that RNA folding can be divided into two classes. To examine this division, folding rates of circularly permutated isomers are compared for two RNAs, one from each class. Folding rates vary by tenfold for circularly permuted Bacillus subtilis RNase P RNA isomers, whereas folding rates vary by only 1.2-fold for circularly permuted catalytic domains. This difference is likely related to the dissimilar natures of their rate-limiting steps.

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Year:  2004        PMID: 15364565     DOI: 10.1016/j.jmb.2004.08.002

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  13 in total

1.  Chain length determines the folding rates of RNA.

Authors:  Changbong Hyeon; D Thirumalai
Journal:  Biophys J       Date:  2012-02-07       Impact factor: 4.033

2.  Developing three-dimensional models of putative-folding intermediates of the HDV ribozyme.

Authors:  Cédric Reymond; Dominique Lévesque; Martin Bisaillon; Jean-Pierre Perreault
Journal:  Structure       Date:  2010-12-08       Impact factor: 5.006

3.  Distinct contribution of electrostatics, initial conformational ensemble, and macromolecular stability in RNA folding.

Authors:  Alain Laederach; Inna Shcherbakova; Magdalena A Jonikas; Russ B Altman; Michael Brenowitz
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-16       Impact factor: 11.205

Review 4.  Informatics challenges in structured RNA.

Authors:  Alain Laederach
Journal:  Brief Bioinform       Date:  2007-07-04       Impact factor: 11.622

5.  A comparison of the folding kinetics of a small, artificially selected DNA aptamer with those of equivalently simple naturally occurring proteins.

Authors:  Camille Lawrence; Alexis Vallée-Bélisle; Shawn H Pfeil; Derek de Mornay; Everett A Lipman; Kevin W Plaxco
Journal:  Protein Sci       Date:  2013-11-28       Impact factor: 6.725

Review 6.  Kinetic barriers and the role of topology in protein and RNA folding.

Authors:  Tobin R Sosnick
Journal:  Protein Sci       Date:  2008-05-23       Impact factor: 6.725

7.  RNA molecules with conserved catalytic cores but variable peripheries fold along unique energetically optimized pathways.

Authors:  Somdeb Mitra; Alain Laederach; Barbara L Golden; Russ B Altman; Michael Brenowitz
Journal:  RNA       Date:  2011-06-28       Impact factor: 4.942

8.  Kinetic and thermodynamic framework for P4-P6 RNA reveals tertiary motif modularity and modulation of the folding preferred pathway.

Authors:  Namita Bisaria; Max Greenfeld; Charles Limouse; Dmitri S Pavlichin; Hideo Mabuchi; Daniel Herschlag
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-04       Impact factor: 11.205

9.  Quantitative tests of a reconstitution model for RNA folding thermodynamics and kinetics.

Authors:  Namita Bisaria; Max Greenfeld; Charles Limouse; Hideo Mabuchi; Daniel Herschlag
Journal:  Proc Natl Acad Sci U S A       Date:  2017-08-24       Impact factor: 11.205

10.  A kinetic intermediate that regulates proper folding of a group II intron RNA.

Authors:  Christina Waldsich; Anna Marie Pyle
Journal:  J Mol Biol       Date:  2007-10-24       Impact factor: 5.469

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