Literature DB >> 11352576

Probing the folding landscape of the Tetrahymena ribozyme: commitment to form the native conformation is late in the folding pathway.

R Russell1, D Herschlag.   

Abstract

Large, structured RNAs traverse folding landscapes in which intermediates and long-lived misfolded states are common. To obtain a comprehensive description of the folding landscape for a structured RNA, it is necessary to understand the connections between productive folding pathways and pathways to these misfolded states. The Tetrahymena group I ribozyme partitions between folding to the native state and to a long-lived misfolded conformation. Here, we show that the observed rate constant for commitment to fold to the native or misfolded states is 1.9 min(-1) (37 degrees C, 10 mM Mg(2+)), the same within error as the rate constant for overall folding to the native state. Thus, the commitment to alternative folding pathways is made late in the folding process, concomitant with or after the rate-limiting step for overall folding. The ribozyme forms much of its tertiary structure significantly faster than it reaches this commitment point and the tertiary structure is expected to be stable, suggesting that the commitment to fold along pathways to the native or misfolded states is made from a partially structured intermediate. These results allow the misfolded conformation to be incorporated into a folding framework that reconciles previous data and gives quantitative information about the energetic topology of the folding landscape for this RNA. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11352576     DOI: 10.1006/jmbi.2001.4751

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


  62 in total

1.  Exploring the folding landscape of a structured RNA.

Authors:  Rick Russell; Xiaowei Zhuang; Hazen P Babcock; Ian S Millett; Sebastian Doniach; Steven Chu; Daniel Herschlag
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-26       Impact factor: 11.205

2.  Rapid compaction during RNA folding.

Authors:  Rick Russell; Ian S Millett; Mark W Tate; Lisa W Kwok; Bradley Nakatani; Sol M Gruner; Simon G J Mochrie; Vijay Pande; Sebastian Doniach; Daniel Herschlag; Lois Pollack
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-02       Impact factor: 11.205

3.  The rate-limiting step in the folding of a large ribozyme without kinetic traps.

Authors:  X-W Fang; P Thiyagarajan; T R Sosnick; T Pan
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-25       Impact factor: 11.205

4.  RNA chaperone StpA loosens interactions of the tertiary structure in the td group I intron in vivo.

Authors:  Christina Waldsich; Rupert Grossberger; Renée Schroeder
Journal:  Genes Dev       Date:  2002-09-01       Impact factor: 11.361

5.  Trypanosoma brucei 20 S editosomes have one RNA substrate-binding site and execute RNA unwinding activity.

Authors:  Cordula Böhm; Venkata Subbaraju Katari; Michael Brecht; H Ulrich Göringer
Journal:  J Biol Chem       Date:  2012-06-01       Impact factor: 5.157

6.  Turning limited experimental information into 3D models of RNA.

Authors:  Samuel Coulbourn Flores; Russ B Altman
Journal:  RNA       Date:  2010-07-22       Impact factor: 4.942

7.  Time-resolved infrared spectroscopy of RNA folding.

Authors:  Eric B Brauns; R Brian Dyer
Journal:  Biophys J       Date:  2005-08-26       Impact factor: 4.033

8.  Structural specificity conferred by a group I RNA peripheral element.

Authors:  Travis H Johnson; Pilar Tijerina; Amanda B Chadee; Daniel Herschlag; Rick Russell
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-11       Impact factor: 11.205

9.  Local kinetic measures of macromolecular structure reveal partitioning among multiple parallel pathways from the earliest steps in the folding of a large RNA molecule.

Authors:  Alain Laederach; Inna Shcherbakova; Mike P Liang; Michael Brenowitz; Russ B Altman
Journal:  J Mol Biol       Date:  2006-03-30       Impact factor: 5.469

10.  Nonspecific binding to structured RNA and preferential unwinding of an exposed helix by the CYT-19 protein, a DEAD-box RNA chaperone.

Authors:  Pilar Tijerina; Hari Bhaskaran; Rick Russell
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-30       Impact factor: 11.205

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