Literature DB >> 21136328

Full matrix Analysis of Cross-relaxation Fails in Fractionally Deuterated Molecules.

Z Zolnai1, N Juranić, S Macura.   

Abstract

We have analyzed cross-relaxation in fractionally deuterated molecules and showed that the full matrix analysis fails except when the dilution is extreme. This is because the isotopic dilution alters the matrix exponential relationship between the observed spectrum and the cross-relaxation rate constants sought. Consequently, an average of the spectra of various isotopomers differs from the matrix exponential of an average relaxation matrix. We have derived a series expansion that allows the determination of the cross-relaxation rate constants in arbitrarily deuterated molecules.

Year:  1998        PMID: 21136328     DOI: 10.1023/A:1008272628775

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


  1 in total

1.  A novel application of nuclear Overhauser enhancement (NOE) in proteins: analysis of correlated events in the exchange of internal labile protons.

Authors:  G Wagner
Journal:  Biochem Biophys Res Commun       Date:  1980-11-28       Impact factor: 3.575

  1 in total
  2 in total

1.  Intermolecular relaxation has little effect on intra-peptide exchange-transferred NOE intensities.

Authors:  Adam P R Zabell; Carol Beth Post
Journal:  J Biomol NMR       Date:  2002-04       Impact factor: 2.835

2.  Sugar conformation of a stereospecific 2'-R or 2'-S deuterium-labeled DNA decamer studied with proton-proton J coupling constants.

Authors:  C Kojima; E Kawashima; T Sekine; Y Ishido; A Ono; M Kainosho; Y Kyogoku
Journal:  J Biomol NMR       Date:  2001-01       Impact factor: 2.835

  2 in total

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