Literature DB >> 21442607

Solution structure of an alternate conformation of helix27 from Escherichia coli16S rRNA.

Meredith Newby Spano1, Nils G Walter.   

Abstract

Helix (H)27 of 16S ribosomal (r)RNA from Escherichia coli was dubbed the "switch helix" when mutagenesis suggested that two alternative base pair registers may have distinct functional roles in the bacterial ribosome. Although more recent genetic analyses suggest that H27 conformational switching is not required for translation, previous solution studies demonstrated that the isolated E. coli H27 can dynamically convert between the 885 and 888 conformations. Here, we have solved the nuclear magnetic resonance solution structure of a locked 888 conformation. NOE and residual dipolar coupling restraints reveal an architecture that markedly differs from that of the 885 conformation found in crystal structures of the bacterial ribosome. In place of the loop E motif that characterizes the 885 conformer and that the 888 conformer cannot adopt, we find evidence for an asymmetrical A-rich internal loop stabilized by stacking interactions among the unpaired A's. Comparison of the isolated H27 888 solution structure with the 885 crystal structure within the context of the ribosome suggests a difference in overall length of H27 that presents one plausible reason for the absence of H27 conformational switching within the sterically confining ribosome.
Copyright © 2011 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21442607      PMCID: PMC3145048          DOI: 10.1002/bip.21626

Source DB:  PubMed          Journal:  Biopolymers        ISSN: 0006-3525            Impact factor:   2.505


  51 in total

1.  Intramolecular secondary structure rearrangement by the kissing interaction of the Neurospora VS ribozyme.

Authors:  A A Andersen; R A Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-26       Impact factor: 11.205

2.  Recognition of cognate transfer RNA by the 30S ribosomal subunit.

Authors:  J M Ogle; D E Brodersen; W M Clemons ; M J Tarry; A P Carter; V Ramakrishnan
Journal:  Science       Date:  2001-05-04       Impact factor: 47.728

3.  Solution structure of Cobalt(III)hexammine complexed to the GAAA tetraloop, and metal-ion binding to G.A mismatches.

Authors:  S Rüdisser; I Tinoco
Journal:  J Mol Biol       Date:  2000-02-04       Impact factor: 5.469

4.  The Xplor-NIH NMR molecular structure determination package.

Authors:  Charles D Schwieters; John J Kuszewski; Nico Tjandra; G Marius Clore
Journal:  J Magn Reson       Date:  2003-01       Impact factor: 2.229

5.  A common motif organizes the structure of multi-helix loops in 16 S and 23 S ribosomal RNAs.

Authors:  N B Leontis; E Westhof
Journal:  J Mol Biol       Date:  1998-10-30       Impact factor: 5.469

6.  A network of heterogeneous hydrogen bonds in GNRA tetraloops.

Authors:  F M Jucker; H A Heus; P F Yip; E H Moors; A Pardi
Journal:  J Mol Biol       Date:  1996-12-20       Impact factor: 5.469

7.  NMRPipe: a multidimensional spectral processing system based on UNIX pipes.

Authors:  F Delaglio; S Grzesiek; G W Vuister; G Zhu; J Pfeifer; A Bax
Journal:  J Biomol NMR       Date:  1995-11       Impact factor: 2.835

8.  Metal interactions with a GAAA RNA tetraloop characterized by (31)P NMR and phosphorothioate substitutions.

Authors:  M Maderia; T E Horton; V J DeRose
Journal:  Biochemistry       Date:  2000-07-18       Impact factor: 3.162

9.  Solution structure and thermodynamics of a divalent metal ion binding site in an RNA pseudoknot.

Authors:  R L Gonzalez; I Tinoco
Journal:  J Mol Biol       Date:  1999-06-25       Impact factor: 5.469

10.  Formation of the central pseudoknot in 16S rRNA is essential for initiation of translation.

Authors:  M F Brink; M P Verbeet; H A de Boer
Journal:  EMBO J       Date:  1993-10       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.