A four-way junction accelerates hairpin ribozyme folding via a discrete intermediate

被引:161
作者
Tan, E
Wilson, TJ
Nahas, MK
Clegg, RM
Lilley, DMJ [1 ]
Ha, T
机构
[1] Univ Dundee, Dept Biochem, Canc Res UK, Nucl Acid Struct Res Grp, Dundee DD1 5EH, Scotland
[2] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[3] Univ Illinois, Ctr Biophys & Computat Biol, Urbana, IL 61801 USA
关键词
D O I
10.1073/pnas.1233536100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The natural form of the hairpin ribozyme comprises two major structural elements: a four-way RNA junction and two internal loops carried by adjacent arms of the junction. The ribozyme folds into its active conformation by an intimate association between the loops, and the efficiency of this process is greatly enhanced by the presence of the junction. We have used single-molecule spectroscopy to show that the natural form fluctuates among three distinct states: the folded state and two additional, rapidly interconverting states (proximal and distal) that are inherited from the junction. The proximal state juxtaposes the two loop elements, thereby increasing the probability of their interaction and thus accelerating folding by nearly three orders of magnitude and allowing the ribozyme to fold rapidly in physiological conditions. Therefore, the hairpin ribozyme exploits the dynamics of the junction to facilitate the formation of the active site from its other elements. Dynamic interplay between structural elements, as we demonstrate for the hairpin ribozyme, may be a general theme for other functional RNA molecules.
引用
收藏
页码:9308 / 9313
页数:6
相关论文
共 28 条
[1]   ESSENTIAL NUCLEOTIDE-SEQUENCES AND SECONDARY STRUCTURE ELEMENTS OF THE HAIRPIN RIBOZYME [J].
BERZALHERRANZ, A ;
JOSEPH, S ;
CHOWRIRA, BM ;
BUTCHER, SE ;
BURKE, JM .
EMBO JOURNAL, 1993, 12 (06) :2567-2574
[2]  
Butcher SE, 1999, NAT STRUCT BIOL, V6, P212
[3]   Solution structure of loop a from the hairpin ribozyme from tobacco ringspot virus satellite [J].
Cai, ZP ;
Tinoco, I .
BIOCHEMISTRY, 1996, 35 (19) :6026-6036
[4]   Single-molecule protein folding: Diffusion fluorescence resonance energy transfer studies of the denaturation of chymotrypsin inhibitor 2 [J].
Deniz, AA ;
Laurence, TA ;
Beligere, GS ;
Dahan, M ;
Martin, AB ;
Chemla, DS ;
Dawson, PE ;
Schultz, PG ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5179-5184
[5]   The chemical repertoire of natural ribozymes [J].
Doudna, JA ;
Cech, TR .
NATURE, 2002, 418 (6894) :222-228
[6]   Tertiary structure stabilization promotes hairpin ribozyme ligation [J].
Fedor, MJ .
BIOCHEMISTRY, 1999, 38 (34) :11040-11050
[7]   Probing the interaction between two single molecules: Fluorescence resonance energy transfer between a single donor and a single acceptor [J].
Ha, T ;
Enderle, T ;
Ogletree, DF ;
Chemla, DS ;
Selvin, PR ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (13) :6264-6268
[8]   Initiation and re-initiation of DNA unwinding by the Escherichia coli Rep helicase [J].
Ha, T ;
Rasnik, I ;
Cheng, W ;
Babcock, HP ;
Gauss, GH ;
Lohman, TM ;
Chu, S .
NATURE, 2002, 419 (6907) :638-641
[9]   Single-molecule fluorescence spectroscopy of enzyme conformational dynamics and cleavage mechanism [J].
Ha, TJ ;
Ting, AY ;
Liang, J ;
Caldwell, WB ;
Deniz, AA ;
Chemla, DS ;
Schultz, PG ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :893-898
[10]   Mg2+-dependent conformational change of RNA studied by fluorescence correlation and FRET on immobilized single molecules [J].
Kim, HD ;
Nienhaus, GU ;
Ha, T ;
Orr, JW ;
Williamson, JR ;
Chu, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4284-4289