Literature DB >> 16009587

Improvement of duty-cycle heating compensation in NMR spin relaxation experiments.

Grover N B Yip1, Erik R P Zuiderweg.   

Abstract

To reliably measure NMR relaxation properties of macromolecules is a prerequisite for precise experiments that identify subtle variations in relaxation rates, as required for the determination of rotational diffusion anisotropy, CSA tensor determination, advanced motional modeling or entropy difference estimations. An underlying problem with current NMR relaxation measurement protocols is maintaining constant sample temperature throughout the execution of the relaxation series especially when rapid data acquisition is required. Here, it is proposed to use a combination of a heating compensation and a proton saturation sequence at the beginning of the NMR relaxation pulse scheme. This simple extension allows reproducible, robust and rapid acquisition of NMR spin relaxation data sets. The method is verified with (15)N spin relaxation measurements for human ubiquitin.

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Year:  2005        PMID: 16009587     DOI: 10.1016/j.jmr.2005.06.003

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  18 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-21       Impact factor: 11.205

4.  Simple tests for the validation of multiple field spin relaxation data.

Authors:  Sébastien Morin; Stéphane M Gagné
Journal:  J Biomol NMR       Date:  2009-10-20       Impact factor: 2.835

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Authors:  Federica De Leo; Giacomo Quilici; Mario Tirone; Francesco De Marchis; Valeria Mannella; Chiara Zucchelli; Alessandro Preti; Alessandro Gori; Maura Casalgrandi; Rosanna Mezzapelle; Marco E Bianchi; Giovanna Musco
Journal:  EMBO Rep       Date:  2019-08-14       Impact factor: 8.807

6.  Improving the quality of oriented membrane protein spectra using heat-compensated separated local field experiments.

Authors:  Songlin Wang; T Gopinath; Gianluigi Veglia
Journal:  J Biomol NMR       Date:  2019-08-28       Impact factor: 2.835

7.  A study on the influence of fast amide exchange on the accuracy of (15)N relaxation rate constants.

Authors:  Simon Jurt; Oliver Zerbe
Journal:  J Biomol NMR       Date:  2012-11-10       Impact factor: 2.835

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Review 9.  An introduction to NMR-based approaches for measuring protein dynamics.

Authors:  Ian R Kleckner; Mark P Foster
Journal:  Biochim Biophys Acta       Date:  2010-11-06

10.  The structure of the KlcA and ArdB proteins reveals a novel fold and antirestriction activity against Type I DNA restriction systems in vivo but not in vitro.

Authors:  Dimitra Serfiotis-Mitsa; Andrew P Herbert; Gareth A Roberts; Dinesh C Soares; John H White; Garry W Blakely; Dusan Uhrín; David T F Dryden
Journal:  Nucleic Acids Res       Date:  2009-12-09       Impact factor: 16.971

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