Literature DB >> 9566314

Improved distance analysis in RNA using network-editing techniques for overcoming errors due to spin diffusion.

C G Hoogstraten1, A Pardi.   

Abstract

Multispin magnetization transfer, or spin diffusion, is a significant source of error in NOESY-derived distance measurements for the determination of nucleic acid solution structures. The BD-NOESY and CBD-NOESY experiments, which allow the measurement of interproton distances with greatly reduced contributions from spin diffusion, have been adapted to structural analysis in RNA oligonucleotides. The techniques are applied to a lead-dependent ribozyme (LZ2). We demonstrate the measurement of both aromatic proton-aromatic proton NOEs free of spin diffusion involving the intervening ribose moieties and aromatic proton-ribose proton NOEs free of the efficient cross-relaxation within the ribose ring. In LZ2, the accuracy and precision of the resulting distances are significantly improved. We also find that, by allowing the use of longer mixing times with greater sensitivity, the experimental attenuation of spin diffusion in RNA increases the distance range of interactions that can be analyzed. This effect permits measurement of important long-range distances in LZ2 that are not accessible with standard techniques. Thus, these techniques allow the simultaneous optimization of the number, accuracy, and precision of distance constraints used for RNA structure determinations.

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Year:  1998        PMID: 9566314     DOI: 10.1023/a:1008239625802

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  11 in total

1.  In vitro selection of RNAs that undergo autolytic cleavage with Pb2+.

Authors:  T Pan; O C Uhlenbeck
Journal:  Biochemistry       Date:  1992-04-28       Impact factor: 3.162

2.  A small metalloribozyme with a two-step mechanism.

Authors:  T Pan; O C Uhlenbeck
Journal:  Nature       Date:  1992-08-13       Impact factor: 49.962

3.  Structures of larger proteins in solution: three- and four-dimensional heteronuclear NMR spectroscopy.

Authors:  G M Clore; A M Gronenborn
Journal:  Science       Date:  1991-06-07       Impact factor: 47.728

4.  The conformation of NAD+ bound to lactate dehydrogenase determined by nuclear magnetic resonance with suppression of spin diffusion.

Authors:  S J Vincent; C Zwahlen; C B Post; J W Burgner; G Bodenhausen
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-29       Impact factor: 11.205

5.  Suppression of spin diffusion in selected frequency bands of nuclear Overhauser spectra.

Authors:  S J Vincent; C Zwahlen; G Bodenhausen
Journal:  J Biomol NMR       Date:  1996-03       Impact factor: 2.835

6.  Comparison of the accuracy of protein solution structures derived from conventional and network-edited NOESY data.

Authors:  C G Hoogstraten; S Choe; W M Westler; J L Markley
Journal:  Protein Sci       Date:  1995-11       Impact factor: 6.725

Review 7.  Two-dimensional exchange spectroscopy of proteins.

Authors:  S Macura; W M Westler; J L Markley
Journal:  Methods Enzymol       Date:  1994       Impact factor: 1.600

8.  Three-dimensional structure of a hammerhead ribozyme.

Authors:  H W Pley; K M Flaherty; D B McKay
Journal:  Nature       Date:  1994-11-03       Impact factor: 49.962

9.  Preparation of 13C and 15N labelled RNAs for heteronuclear multi-dimensional NMR studies.

Authors:  E P Nikonowicz; A Sirr; P Legault; F M Jucker; L M Baer; A Pardi
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

10.  Properties of an in vitro selected Pb2+ cleavage motif.

Authors:  T Pan; B Dichtl; O C Uhlenbeck
Journal:  Biochemistry       Date:  1994-08-16       Impact factor: 3.162

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