RNA helical packing in solution: NMR structure of a 30 kDa GAAA tetraloop-receptor complex

被引:110
作者
Davis, JH
Tonelli, M
Scott, LG
Jaeger, L
Williamson, JR
Butcher, SE
机构
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[2] Univ Wisconsin, Nucl Magnet Resonance Fac Madison, Madison, WI 53706 USA
[3] Scripps Res Inst, Dept Mol Biol, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[4] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
关键词
NMR; RNA tertiary structure; GAAA tetraloop; 11-nucleoticle receptor; RNA helical packing;
D O I
10.1016/j.jmb.2005.05.069
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
Tertiary interactions are critical for proper RNA folding and ribozyme catalysis. RNA tertiary structure is often condensed through long-range helical packing interactions mediated by loop-receptor motifs. RNA structures displaying helical packing by loop-receptor interactions have been solved by X-ray crystallography, but not by NMR. Here, we report the NMR structure of a 30 kDa GAAA tetraloop-receptor RNA complex. In order to stabilize the complex, we used a modular design in which the RNA was engineered to form a homodimer, with each subunit containing a GAAA tetraloop phased one helical turn apart from its cognate 11-nucleotide receptor domain. The structure determination utilized specific isotopic labeling patterns (H-2, C-13 and N-15) and refinement against residual dipolar couplings. We observe a unique and highly unusual chemical shift pattern for an adenosine platform interaction that reveals a spectroscopic fingerprint for this motif. The structure of the GAAA tetraloop-receptor interaction is well defined solely from experimental NMR data, shows minor deviations from previously solved crystal structures, and verifies the previously inferred hydrogen bonding patterns within this motif. This work demonstrates the feasibility of using engineered homodimers as modular systems for the determination of RNA tertiary interactions by NMR. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:371 / 382
页数:12
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共 60 条
[11]   The two faces of the Escherichia coli 23 S rRNA sarcin/ricin domain:: The structure at 1.11 Å resolution [J].
Correll, CC ;
Wool, IG ;
Munishkin, A .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (02) :275-287
[12]   FREQUENT USE OF THE SAME TERTIARY MOTIF BY SELF-FOLDING RNAS [J].
COSTA, M ;
MICHEL, F .
EMBO JOURNAL, 1995, 14 (06) :1276-1285
[13]   NMR structure of the 101-nucleotide core encapsidation signal of the Moloney murine leukemia virus [J].
D'Souza, V ;
Dey, A ;
Habib, D ;
Summers, MF .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 337 (02) :427-442
[14]   Structural basis for packaging the dimeric genome of Moloney murine leukaemia virus [J].
D'Souza, V ;
Summers, MF .
NATURE, 2004, 431 (7008) :586-590
[15]   NMRPIPE - A MULTIDIMENSIONAL SPECTRAL PROCESSING SYSTEM BASED ON UNIX PIPES [J].
DELAGLIO, F ;
GRZESIEK, S ;
VUISTER, GW ;
ZHU, G ;
PFEIFER, J ;
BAX, A .
JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (03) :277-293
[16]   Direct observation of hydrogen bonds in nucleic acid base pairs by internucleotide 2JNN couplings [J].
Dingley, AJ ;
Grzesiek, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (33) :8293-8297
[17]   Emerging themes in RNA folding [J].
Doudna, JA ;
Doherty, EA .
FOLDING & DESIGN, 1997, 2 (05) :R65-R70
[18]   The chemical repertoire of natural ribozymes [J].
Doudna, JA ;
Cech, TR .
NATURE, 2002, 418 (6894) :222-228
[19]   The synthesis of deuterionucleosides [J].
Földesi, A ;
Trifonova, A ;
Kundu, MK ;
Chattopadhyaya, J .
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2000, 19 (10-12) :1615-1656
[20]   A preorganized active site in the crystal structure of the Tetrahymena ribozyme [J].
Golden, BL ;
Gooding, AR ;
Podell, ER ;
Cech, TR .
SCIENCE, 1998, 282 (5387) :259-264