Literature DB >> 11414851

Comparison of methyl rotation axis order parameters derived from model-free analyses of (2)H and (13)C longitudinal and transverse relaxation rates measured in the same protein sample.

R Ishima1, A P Petkova, J M Louis, D A Torchia.   

Abstract

Recombinant HIV-1 protease was obtained from bacteria grown on a 98% D(2)O medium containing 3-(13)C pyruvic acid as the sole source of (13)C and (1)H. The purified protein is highly deuterated at non-methyl carbons, but contains significant populations of (13)CHD(2) and (13)CH(2)D methyl isotopomers. This pattern of isotope labeling permitted measurements of (1)H and (13)C relaxation rates of (13)CHD(2) isotopomers and (2)H (D) relaxation rates of (13)CH(2)D isotopomers using a single sample. The order parameters S(axis)(2), which characterize the motions of the methyl rotation axes, were derived from model-free analyses of R(1) and R(2) data sets measured for (13)C and (2)H spins. Our primary goal was to compare the S(axis)(2) values derived from the two independent types of data sets to test our understanding of the relaxation mechanisms involved. However, S(axis)(2) values derived from the analyses depend strongly on the geometry of the methyl group, the sizes of the quadrupolar and dipolar couplings, and the effects of bond vibrations and librations on these couplings. Therefore uncertainties in these basic physical parameters complicate comparison of the order parameters. This problem was circumvented by using an experimental relationship, between the methyl quadrupolar, (13)C-(13)C and (13)C-(1)H dipolar couplings, derived from independent measurements of residual static couplings of weakly aligned proteins by Ottiger and Bax (J. Am. Chem. Soc. 1999, 121, 4690-4695) and Mittermaier and Kay (J. Am. Chem. Soc. 1999, 121, 10608-10613). This approach placed a tight experimental restraint on the values of the (2)H quadrupolar and (13)C-(1)H dipolar interactions and greatly facilitated the accurate comparison of the relative values of the order parameters. When applied to our data this approach yielded satisfactory agreement between the S(axis)(2) values derived from the (13)C and (2)H data sets.

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Year:  2001        PMID: 11414851     DOI: 10.1021/ja0104711

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  29 in total

1.  Optimized labeling of 13CHD2 methyl isotopomers in perdeuterated proteins: potential advantages for 13C relaxation studies of methyl dynamics of larger proteins.

Authors:  R Ishima; J M Louis; D A Torchia
Journal:  J Biomol NMR       Date:  2001-10       Impact factor: 2.835

2.  Prediction of methyl-side chain dynamics in proteins.

Authors:  Dengming Ming; Rafael Brüschweiler
Journal:  J Biomol NMR       Date:  2004-07       Impact factor: 2.835

3.  Estimating side-chain order in methyl-protonated, perdeuterated proteins via multiple-quantum relaxation violated coherence transfer NMR spectroscopy.

Authors:  Hechao Sun; Raquel Godoy-Ruiz; Vitali Tugarinov
Journal:  J Biomol NMR       Date:  2012-03       Impact factor: 2.835

Review 4.  Characterization of the fast dynamics of protein amino acid side chains using NMR relaxation in solution.

Authors:  Tatyana I Igumenova; Kendra King Frederick; A Joshua Wand
Journal:  Chem Rev       Date:  2006-05       Impact factor: 60.622

Review 5.  NMR studies of dynamic biomolecular conformational ensembles.

Authors:  Dennis A Torchia
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2014-11-28       Impact factor: 9.795

6.  Intrinsic dynamics of the partly unstructured PX domain from the Sendai virus RNA polymerase cofactor P.

Authors:  Klaartje Houben; Laurence Blanchard; Martin Blackledge; Dominique Marion
Journal:  Biophys J       Date:  2007-06-22       Impact factor: 4.033

7.  Generation and relaxation of high rank coherences in AX3 systems in a selectively methionine labelled SH2 domain.

Authors:  Karin Kloiber; Michael Fischer; Karin Ledolter; Michael Nagl; Walther Schmid; Robert Konrat
Journal:  J Biomol NMR       Date:  2007-05-09       Impact factor: 2.835

8.  Site-specific analysis of heteronuclear Overhauser effects in microcrystalline proteins.

Authors:  Juan Miguel Lopez del Amo; Vipin Agarwal; Riddhiman Sarkar; Justin Porter; Sam Asami; Martin Rübbelke; Uwe Fink; Yi Xue; Oliver F Lange; Bernd Reif
Journal:  J Biomol NMR       Date:  2014-07-03       Impact factor: 2.835

9.  Measurement of methyl 13C-1H cross-correlation in uniformly 13C-, 15N-, labeled proteins.

Authors:  Weidong Liu; Yu Zheng; David P Cistola; Daiwen Yang
Journal:  J Biomol NMR       Date:  2003-12       Impact factor: 2.835

Review 10.  A surprising role for conformational entropy in protein function.

Authors:  A Joshua Wand; Veronica R Moorman; Kyle W Harpole
Journal:  Top Curr Chem       Date:  2013
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