Literature DB >> 11276255

A universal mode of helix packing in RNA.

E A Doherty1, R T Batey, B Masquida, J A Doudna.   

Abstract

RNA molecules fold into specific three-dimensional shapes to perform structural and catalytic functions. Large RNAs can form compact globular structures, but the chemical basis for close helical packing within these molecules has been unclear. Analysis of transfer, catalysis, in vitro-selected and ribosomal RNAs reveal that helical packing predominantly involves the interaction of single-stranded adenosines with a helix minor groove. Using the Tetrahymena thermophila group I ribozyme, we show here that the near-perfect shape complementarity between the adenine base and the minor groove allows for optimal van der Waals contacts, extensive hydrogen bonding and hydrophobic surface burial, creating a highly energetically favorable interaction. Adenosine is recognized in a chemically similar fashion by a combination of protein and RNA components in the ribonucleoprotein core of the signal recognition particle. These results provide a thermodynamic explanation for the noted abundance of conserved adenosines within the unpaired regions of RNA secondary structures.

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Year:  2001        PMID: 11276255     DOI: 10.1038/86221

Source DB:  PubMed          Journal:  Nat Struct Biol        ISSN: 1072-8368


  100 in total

1.  NMR structure of a ribosomal RNA hairpin containing a conserved CUCAA pentaloop.

Authors:  U Nagaswamy; X Gao; S A Martinis; G E Fox
Journal:  Nucleic Acids Res       Date:  2001-12-15       Impact factor: 16.971

2.  Common and distinctive features of GNRA tetraloops based on a GUAA tetraloop structure at 1.4 A resolution.

Authors:  Carl C Correll; Kerren Swinger
Journal:  RNA       Date:  2003-03       Impact factor: 4.942

3.  Structural organization of a viral IRES depends on the integrity of the GNRA motif.

Authors:  Olga Fernández-Miragall; Encarnación Martínez-Salas
Journal:  RNA       Date:  2003-11       Impact factor: 4.942

4.  The common and the distinctive features of the bulged-G motif based on a 1.04 A resolution RNA structure.

Authors:  Carl C Correll; Jutta Beneken; Matthew J Plantinga; Melissa Lubbers; Yuen-Ling Chan
Journal:  Nucleic Acids Res       Date:  2003-12-01       Impact factor: 16.971

5.  GU receptors of double helices mediate tRNA movement in the ribosome.

Authors:  Matthieu G Gagnon; Sergey V Steinberg
Journal:  RNA       Date:  2002-07       Impact factor: 4.942

6.  Specificity of RNA-RNA helix recognition.

Authors:  Daniel J Battle; Jennifer A Doudna
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-20       Impact factor: 11.205

7.  Parameter optimized surfaces (POPS): analysis of key interactions and conformational changes in the ribosome.

Authors:  Franca Fraternali; Luigi Cavallo
Journal:  Nucleic Acids Res       Date:  2002-07-01       Impact factor: 16.971

8.  On the occurrence of the T-loop RNA folding motif in large RNA molecules.

Authors:  Andrey S Krasilnikov; Alfonso Mondragón
Journal:  RNA       Date:  2003-06       Impact factor: 4.942

9.  Representation, searching and discovery of patterns of bases in complex RNA structures.

Authors:  Anne-Marie Harrison; Darren R South; Peter Willett; Peter J Artymiuk
Journal:  J Comput Aided Mol Des       Date:  2003-08       Impact factor: 3.686

10.  Monitoring intermediate folding states of the td group I intron in vivo.

Authors:  Christina Waldsich; Benoît Masquida; Eric Westhof; Renée Schroeder
Journal:  EMBO J       Date:  2002-10-01       Impact factor: 11.598

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