Literature DB >> 12766391

Chemical shift-dependent apparent scalar couplings: an alternative concept of chemical shift monitoring in multi-dimensional NMR experiments.

Witek Kwiatkowski1, Roland Riek.   

Abstract

The paper presents an alternative technique for chemical shift monitoring in a multi-dimensional NMR experiment. The monitored chemical shift is coded in the line-shape of a cross-peak through an apparent residual scalar coupling active during an established evolution period or acquisition. The size of the apparent scalar coupling is manipulated with an off-resonance radio-frequency pulse in order to correlate the size of the coupling with the position of the additional chemical shift. The strength of this concept is that chemical shift information is added without an additional evolution period and accompanying polarization transfer periods. This concept was incorporated into the three-dimensional triple-resonance experiment HNCA, adding the information of (1)H(alpha) chemical shifts. The experiment is called HNCA(coded)HA, since the chemical shift of (1)H(alpha) is coded in the line-shape of the cross-peak along the (13)C(alpha) dimension.

Mesh:

Substances:

Year:  2003        PMID: 12766391     DOI: 10.1023/a:1023083911125

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


  10 in total

1.  TROSY and CRINEPT: NMR with large molecular and supramolecular structures in solution.

Authors:  R Riek; K Pervushin; K Wüthrich
Journal:  Trends Biochem Sci       Date:  2000-10       Impact factor: 13.807

Review 2.  Protein NMR spectroscopy in structural genomics.

Authors:  G T Montelione; D Zheng; Y J Huang; K C Gunsalus; T Szyperski
Journal:  Nat Struct Biol       Date:  2000-11

Review 3.  Mapping protein-protein interactions in solution by NMR spectroscopy.

Authors:  Erik R P Zuiderweg
Journal:  Biochemistry       Date:  2002-01-08       Impact factor: 3.162

4.  Rotational diffusion anisotropy of proteins from simultaneous analysis of 15N and 13C alpha nuclear spin relaxation.

Authors:  L K Lee; M Rance; W J Chazin; A G Palmer
Journal:  J Biomol NMR       Date:  1997-04       Impact factor: 2.835

5.  Three-dimensional NMR spectroscopy of a protein in solution.

Authors:  H Oschkinat; C Griesinger; P J Kraulis; O W Sørensen; R R Ernst; A M Gronenborn; G M Clore
Journal:  Nature       Date:  1988-03-24       Impact factor: 49.962

6.  A dipolar coupling based strategy for simultaneous resonance assignment and structure determination of protein backbones.

Authors:  F Tian; H Valafar; J H Prestegard
Journal:  J Am Chem Soc       Date:  2001-11-28       Impact factor: 15.419

7.  Biosynthesis studies with carbon-13. Asperlin.

Authors:  M Tanabe; T Hamasaki; D Thomas; L Johnson
Journal:  J Am Chem Soc       Date:  1971-01-13       Impact factor: 15.419

8.  Attenuated T2 relaxation by mutual cancellation of dipole-dipole coupling and chemical shift anisotropy indicates an avenue to NMR structures of very large biological macromolecules in solution.

Authors:  K Pervushin; R Riek; G Wider; K Wüthrich
Journal:  Proc Natl Acad Sci U S A       Date:  1997-11-11       Impact factor: 11.205

9.  TROSY in triple-resonance experiments: new perspectives for sequential NMR assignment of large proteins.

Authors:  M Salzmann; K Pervushin; G Wider; H Senn; K Wüthrich
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

10.  Four-dimensional heteronuclear triple-resonance NMR spectroscopy of interleukin-1 beta in solution.

Authors:  L E Kay; G M Clore; A Bax; A M Gronenborn
Journal:  Science       Date:  1990-07-27       Impact factor: 47.728

  10 in total
  1 in total

1.  3D TROSY-HNCA(coded)CB and TROSY-HNCA(coded)CO experiments: triple resonance NMR experiments with two sequential connectivity pathways and high sensitivity.

Authors:  Christiane Ritter; Thorsten Lührs; Witek Kwiatkowski; Roland Riek
Journal:  J Biomol NMR       Date:  2004-03       Impact factor: 2.835

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.