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

被引:88
作者
Russell, R [1 ]
Herschlag, D [1 ]
机构
[1] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
关键词
folding landscape; group I intron; misfolding; ribozyme; RNA folding;
D O I
10.1006/jmbi.2001.4751
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
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 degreesC, 10 mM Mg2+), 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. (C) 2001 Academic Press.
引用
收藏
页码:839 / 851
页数:13
相关论文
共 39 条
[1]   DYNAMICS OF RIBOZYME BINDING OF SUBSTRATE REVEALED BY FLUORESCENCE-DETECTED STOPPED-FLOW METHODS [J].
BEVILACQUA, PC ;
KIERZEK, R ;
JOHNSON, KA ;
TURNER, DH .
SCIENCE, 1992, 258 (5086) :1355-1357
[2]   Hierarchy and dynamics of RNA folding [J].
Brion, P ;
Westhof, E .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1997, 26 :113-137
[3]   REPRESENTATION OF THE SECONDARY AND TERTIARY STRUCTURE OF GROUP-I INTRONS [J].
CECH, TR ;
DAMBERGER, SH ;
GUTELL, RR .
NATURE STRUCTURAL BIOLOGY, 1994, 1 (05) :273-280
[4]   Folding mechanism of the Tetrahymena ribozyme P4-P6 domain [J].
Deras, ML ;
Brenowitz, M ;
Ralston, CY ;
Chance, MR ;
Woodson, SA .
BIOCHEMISTRY, 2000, 39 (36) :10975-10985
[5]  
Downs WD, 1996, RNA, V2, P718
[6]   Analysis of rate-determining conformational changes during self-splicing of the Tetrahymena intron [J].
Emerick, VL ;
Pan, J ;
Woodson, SA .
BIOCHEMISTRY, 1996, 35 (41) :13469-13477
[7]   FINGERPRINTING THE FOLDING OF A GROUP-I PRECURSOR RNA [J].
EMERICK, VL ;
WOODSON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) :9675-9679
[8]  
Fersht A, 1999, STRUCTURE MECH PROTE
[9]   EVIDENCE FOR PROCESSIVITY AND 2-STEP BINDING OF THE RNA SUBSTRATE FROM STUDIES OF J1/2 MUTANTS OF THE TETRAHYMENA RIBOZYME [J].
HERSCHLAG, D .
BIOCHEMISTRY, 1992, 31 (05) :1386-1399
[10]   CATALYSIS OF RNA CLEAVAGE BY THE TETRAHYMENA-THERMOPHILA RIBOZYME .1. KINETIC DESCRIPTION OF THE REACTION OF AN RNA SUBSTRATE COMPLEMENTARY TO THE ACTIVE-SITE [J].
HERSCHLAG, D ;
CECH, TR .
BIOCHEMISTRY, 1990, 29 (44) :10159-10171