Literature DB >> 22466935

Quantitative comparison of errors in 15N transverse relaxation rates measured using various CPMG phasing schemes.

Wazo Myint1, Yufeng Cai, Celia A Schiffer, Rieko Ishima.   

Abstract

Nitrogen-15 Carr-Purcell-Meiboom-Gill (CPMG) transverse relaxation experiment are widely used to characterize protein backbone dynamics and chemical exchange parameters. Although an accurate value of the transverse relaxation rate, R(2), is needed for accurate characterization of dynamics, the uncertainty in the R(2) value depends on the experimental settings and the details of the data analysis itself. Here, we present an analysis of the impact of CPMG pulse phase alternation on the accuracy of the (15)N CPMG R(2). Our simulations show that R(2) can be obtained accurately for a relatively wide spectral width, either using the conventional phase cycle or using phase alternation when the r.f. pulse power is accurately calibrated. However, when the r.f. pulse is miscalibrated, the conventional CPMG experiment exhibits more significant uncertainties in R(2) caused by the off-resonance effect than does the phase alternation experiment. Our experiments show that this effect becomes manifest under the circumstance that the systematic error exceeds that arising from experimental noise. Furthermore, our results provide the means to estimate practical parameter settings that yield accurate values of (15)N transverse relaxation rates in the both CPMG experiments.

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Year:  2012        PMID: 22466935      PMCID: PMC4872704          DOI: 10.1007/s10858-012-9621-x

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


  40 in total

1.  Potential bias in NMR relaxation data introduced by peak intensity analysis and curve fitting methods.

Authors:  J H Viles; B M Duggan; E Zaborowski; S Schwarzinger; J J Huntley; G J Kroon; H J Dyson; P E Wright
Journal:  J Biomol NMR       Date:  2001-09       Impact factor: 2.835

Review 2.  NMR studies of protein structure and dynamics.

Authors:  Lewis E Kay
Journal:  J Magn Reson       Date:  2005-04       Impact factor: 2.229

3.  A phase cycle scheme that significantly suppresses offset-dependent artifacts in the R2-CPMG 15N relaxation experiment.

Authors:  Grover N B Yip; Erik R P Zuiderweg
Journal:  J Magn Reson       Date:  2004-11       Impact factor: 2.229

4.  Exact solution of the CPMG pulse sequence with phase variation down the echo train: application to R₂ measurements.

Authors:  Alex D Bain; Christopher Kumar Anand; Zhenghua Nie
Journal:  J Magn Reson       Date:  2011-01-20       Impact factor: 2.229

5.  Insights into the local residual entropy of proteins provided by NMR relaxation.

Authors:  Z Li; S Raychaudhuri; A J Wand
Journal:  Protein Sci       Date:  1996-12       Impact factor: 6.725

6.  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

7.  Rapid structural fluctuations of the free HIV protease flaps in solution: relationship to crystal structures and comparison with predictions of dynamics calculations.

Authors:  Darón I Freedberg; Rieko Ishima; Jaison Jacob; Yun-Xing Wang; Irina Kustanovich; John M Louis; Dennis A Torchia
Journal:  Protein Sci       Date:  2002-02       Impact factor: 6.725

8.  Protein dynamics studied by rotating frame 15N spin relaxation times.

Authors:  T Szyperski; P Luginbühl; G Otting; P Güntert; K Wüthrich
Journal:  J Biomol NMR       Date:  1993-03       Impact factor: 2.835

9.  Crystal structure of lysine sulfonamide inhibitor reveals the displacement of the conserved flap water molecule in human immunodeficiency virus type 1 protease.

Authors:  Madhavi N L Nalam; Anik Peeters; Tim H M Jonckers; Inge Dierynck; Celia A Schiffer
Journal:  J Virol       Date:  2007-06-27       Impact factor: 5.103

10.  Comparison of MD simulations and NMR experiments for hen lysozyme. Analysis of local fluctuations, cooperative motions, and global changes.

Authors:  L J Smith; A E Mark; C M Dobson; W F van Gunsteren
Journal:  Biochemistry       Date:  1995-08-29       Impact factor: 3.162

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  2 in total

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Authors:  Gennady Khirich; J Patrick Loria
Journal:  J Phys Chem B       Date:  2015-02-20       Impact factor: 2.991

2.  Elucidating a relationship between conformational sampling and drug resistance in HIV-1 protease.

Authors:  Ian Mitchelle S de Vera; Adam N Smith; Maria Cristina A Dancel; Xi Huang; Ben M Dunn; Gail E Fanucci
Journal:  Biochemistry       Date:  2013-05-01       Impact factor: 3.162

  2 in total

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