Literature DB >> 11779230

Concerted motions in HIV-1 TAR RNA may allow access to bound state conformations: RNA dynamics from NMR residual dipolar couplings.

Hashim M Al-Hashimi1, Yuying Gosser, Andrey Gorin, Weidong Hu, Ananya Majumdar, Dinshaw J Patel.   

Abstract

Ground-state dynamics in RNA is a critical precursor for structural adaptation observed ubiquitously in protein-RNA recognition. A tertiary conformational analysis of the stem-loop structural element in the transactivation response element (TAR) from human immunodeficiency virus type 1 (HIV-I) RNA is presented using recently introduced NMR methods that rely on the measurement of residual dipolar couplings (RDC) in partially oriented systems. Order matrix analysis of RDC data provides evidence for inter-helical motions that are of amplitude 46(+/-4) degrees, of random directional character, and that are executed about an average conformation with an inter-helical angle between 44 degrees and 54 degrees. The generated ensemble of TAR conformations have different organizations of functional groups responsible for interaction with the trans-activator protein Tat, including conformations similar to the previously characterized bound-state conformation. These results demonstrate the utility of RDC-NMR for simultaneously characterizing RNA tertiary dynamics and average conformation, and indicate an avenue for TAR complex formation involving tertiary structure capture. Copyright 2001 Academic Press.

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Year:  2002        PMID: 11779230     DOI: 10.1006/jmbi.2001.5235

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  72 in total

1.  The solution structure of an essential stem-loop of human telomerase RNA.

Authors:  Thomas Leeper; Nicolas Leulliot; Gabriele Varani
Journal:  Nucleic Acids Res       Date:  2003-05-15       Impact factor: 16.971

2.  Evidence for a base triple in the free HIV-1 TAR RNA.

Authors:  Hendrik Huthoff; Frederic Girard; Sybren S Wijmenga; Ben Berkhout
Journal:  RNA       Date:  2004-03       Impact factor: 4.942

3.  Measuring single-molecule nucleic acid dynamics in solution by two-color filtered ratiometric fluorescence correlation spectroscopy.

Authors:  Haitao Li; Xiaojun Ren; Liming Ying; Shankar Balasubramanian; David Klenerman
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-27       Impact factor: 11.205

4.  Interactions of protein side chains with RNA defined with REDOR solid state NMR.

Authors:  Wei Huang; Gabriele Varani; Gary P Drobny
Journal:  J Biomol NMR       Date:  2011-09-25       Impact factor: 2.835

5.  3D maps of RNA interhelical junctions.

Authors:  Maximillian H Bailor; Anthony M Mustoe; Charles L Brooks; Hashim M Al-Hashimi
Journal:  Nat Protoc       Date:  2011-09-15       Impact factor: 13.491

6.  Changes in DNA bending induced by restricting nucleotide ring pucker studied by weak alignment NMR spectroscopy.

Authors:  Zhengrong Wu; Melissa Maderia; Joseph J Barchi; Victor E Marquez; Ad Bax
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-23       Impact factor: 11.205

7.  Evidence that electrostatic interactions dictate the ligand-induced arrest of RNA global flexibility.

Authors:  Stephen W Pitt; Qi Zhang; Dinshaw J Patel; Hashim M Al-Hashimi
Journal:  Angew Chem Int Ed Engl       Date:  2005-05-30       Impact factor: 15.336

8.  Conformational dynamics of RNA-peptide binding: a molecular dynamics simulation study.

Authors:  Yuguang Mu; Gerhard Stock
Journal:  Biophys J       Date:  2005-10-20       Impact factor: 4.033

9.  Characterizing the relative orientation and dynamics of RNA A-form helices using NMR residual dipolar couplings.

Authors:  Maximillian H Bailor; Catherine Musselman; Alexandar L Hansen; Kush Gulati; Dinshaw J Patel; Hashim M Al-Hashimi
Journal:  Nat Protoc       Date:  2007       Impact factor: 13.491

10.  Measurement and interpretation of 15N-1H residual dipolar couplings in larger proteins.

Authors:  Akash Bhattacharya; Matthew Revington; Erik R P Zuiderweg
Journal:  J Magn Reson       Date:  2009-11-26       Impact factor: 2.229

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