Literature DB >> 8062930

A pulsed field gradient isotope-filtered 3D 13C HMQC-NOESY experiment for extracting intermolecular NOE contacts in molecular complexes.

W Lee1, M J Revington, C Arrowsmith, L E Kay.   

Abstract

A pulsed field gradient three-dimensional isotope-filtered 13C HMQC-NOESY experiment has been developed to characterize intermolecular contacts in a 37 kDa macromolecular ternary complex consisting of uniformly 13C labeled trp-repressor, its natural abundance co-repressor, L-tryptophan, and natural abundance operator DNA. The pulse scheme makes use of pulsed field gradients for the removal of artifacts and dephasing of unwanted magnetization during isotope filtering, and employs a strategy to minimize the time that magnetization resides in the transverse plane. The experiment provides solely intermolecular NOE contacts between protons of the labeled protein and protons of the unlabeled species, and has proven to be especially useful in eliminating ambiguities between intra- and intermolecular NOEs in the isotope-edited 3D 13C HMQC-NOESY spectrum of the complex.

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Year:  1994        PMID: 8062930     DOI: 10.1016/0014-5793(94)00740-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  65 in total

1.  NMR analysis of cleaved Escherichia coli thioredoxin (1-73/74-108) and its P76A variant: cis/trans peptide isomerization.

Authors:  W F Yu; C S Tung; H Wang; M L Tasayco
Journal:  Protein Sci       Date:  2000-01       Impact factor: 6.725

2.  Molecular basis of sequence-specific recognition of pre-ribosomal RNA by nucleolin.

Authors:  F H Allain; P Bouvet; T Dieckmann; J Feigon
Journal:  EMBO J       Date:  2000-12-15       Impact factor: 11.598

3.  Solution structure of the HMG protein NHP6A and its interaction with DNA reveals the structural determinants for non-sequence-specific binding.

Authors:  F H Allain; Y M Yen; J E Masse; P Schultze; T Dieckmann; R C Johnson; J Feigon
Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

4.  NMR structure of the KaiC-interacting C-terminal domain of KaiA, a circadian clock protein: implications for KaiA-KaiC interaction.

Authors:  Ioannis Vakonakis; Jingchuan Sun; Tianfu Wu; Andreas Holzenburg; Susan S Golden; Andy C LiWang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-28       Impact factor: 11.205

5.  Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains.

Authors:  Maria Victoria E Botuyan; Yves Nominé; Xiaochun Yu; Nenad Juranic; Slobodan Macura; Junjie Chen; Georges Mer
Journal:  Structure       Date:  2004-07       Impact factor: 5.006

6.  Structural basis of pre-let-7 miRNA recognition by the zinc knuckles of pluripotency factor Lin28.

Authors:  Fionna E Loughlin; Luca F R Gebert; Harry Towbin; Andreas Brunschweiger; Jonathan Hall; Frédéric H-T Allain
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7.  An improved double-tuned and isotope-filtered pulse scheme based on a pulsed field gradient and a wide-band inversion shaped pulse.

Authors:  K Ogura; H Terasawa; F Inagaki
Journal:  J Biomol NMR       Date:  1996-12       Impact factor: 2.835

Review 8.  Fuzzy complexes of myelin basic protein: NMR spectroscopic investigations of a polymorphic organizational linker of the central nervous system.

Authors:  David S Libich; Mumdooh A M Ahmed; Ligang Zhong; Vladimir V Bamm; Vladimir Ladizhansky; George Harauz
Journal:  Biochem Cell Biol       Date:  2010-04       Impact factor: 3.626

9.  Hydrophobic side-chain size is a determinant of the three-dimensional structure of the p53 oligomerization domain.

Authors:  M McCoy; E S Stavridi; J L Waterman; A M Wieczorek; S J Opella; T D Halazonetis
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

10.  Chemical shift as a probe of molecular interfaces: NMR studies of DNA binding by the three amino-terminal zinc finger domains from transcription factor IIIA.

Authors:  M P Foster; D S Wuttke; K R Clemens; W Jahnke; I Radhakrishnan; L Tennant; M Reymond; J Chung; P E Wright
Journal:  J Biomol NMR       Date:  1998-07       Impact factor: 2.835

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