Literature DB >> 1841707

Effects of internal motions on the development of the two-dimensional transferred nuclear Overhauser effect.

A P Campbell1, B D Sykes.   

Abstract

In this paper we address the influence of internal motions on the development of the transferred nuclear Overhauser effect in a ligand undergoing chemical exchange between a free and a bound state. We examine the effects of varying the effective correlation time as well as the motional order parameter for methyl group and phenyl ring rotations in the free and bound ligand conformations. The effect of decreasing the motional order for a proton pair on a methyl group or phenyl ring is to decrease the effective correlation time of the internuclear vector, and thus to decrease the cross-relaxation rate between the proton pair. This functions to dampen the effects of spin diffusion, especially in the bound ligand where cross-relaxation rates are much faster than in the free ligand. The effect of changing the effective correlation time for methyl group motions has little effect on the build-up behaviour of the transferred nuclear Overhauser effect for small values of fraction bound, but a larger effect on how fast it decays. This effect is greater for internal motions in the free peptide than it is for internal motions in the bound peptide.

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Year:  1991        PMID: 1841707     DOI: 10.1007/bf02192862

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


  22 in total

1.  Conformation of methyl beta-lactoside bound to the ricin B-chain: interpretation of transferred nuclear Overhauser effects facilitated by spin simulation and selective deuteration.

Authors:  V L Bevilacqua; D S Thomson; J H Prestegard
Journal:  Biochemistry       Date:  1990-06-12       Impact factor: 3.162

2.  NMR studies of flexible opiate conformations at monoclonal antibody binding sites. I. Transferred nuclear Overhauser effects show bound conformations.

Authors:  J A Glasel; P N Borer
Journal:  Biochem Biophys Res Commun       Date:  1986-12-30       Impact factor: 3.575

3.  Effect of internal rotation on nuclear magnetic relaxation times for macromolecules.

Authors:  A G Marshall; P G Schmidt; B D Sykes
Journal:  Biochemistry       Date:  1972-10-10       Impact factor: 3.162

4.  Analysis of an enzyme-substrate complex by X-ray crystallography and transferred nuclear Overhauser enhancement measurements: porcine pancreatic elastase and a hexapeptide.

Authors:  E F Meyer; G M Clore; A M Gronenborn; H A Hansen
Journal:  Biochemistry       Date:  1988-01-26       Impact factor: 3.162

5.  Nuclear magnetic resonance studies of flexible opiate conformations at monoclonal antibody binding sites. Quantitative interproton distances obtained from comparing theoretical and experimental transferred nuclear Overhauser enhancement: correlation with antibody sequence.

Authors:  J A Glasel
Journal:  J Mol Biol       Date:  1989-10-20       Impact factor: 5.469

6.  Antibodies against a peptide of cholera toxin differing in cross-reactivity with the toxin differ in their specific interactions with the peptide as observed by 1H NMR spectroscopy.

Authors:  J Anglister; B Zilber
Journal:  Biochemistry       Date:  1990-01-30       Impact factor: 3.162

7.  Nuclear Overhauser effect studies of the conformations and binding site environments of deoxynucleoside triphosphate substrates bound to DNA polymerase I and its large fragment.

Authors:  L J Ferrin; A S Mildvan
Journal:  Biochemistry       Date:  1985-11-19       Impact factor: 3.162

8.  High-resolution NMR studies of fibrinogen-like peptides in solution: structure of a thrombin-bound peptide corresponding to residues 7-16 of the A alpha chain of human fibrinogen.

Authors:  F Ni; Y C Meinwald; M Vásquez; H A Scheraga
Journal:  Biochemistry       Date:  1989-04-04       Impact factor: 3.162

9.  Conformations of the coenzymes and the allosteric activator, ADP, bound to NAD(+)-dependent isocitrate dehydrogenase from pig heart.

Authors:  R S Ehrlich; R F Colman
Journal:  Biochemistry       Date:  1990-05-29       Impact factor: 3.162

10.  Stereochemistry of binding of the tetrapeptide acetyl-Pro-Ala-Pro-Tyr-NH2 to porcine pancreatic elastase. Combined use of two-dimensional transferred nuclear Overhauser enhancement measurements, restrained molecular dynamics, X-ray crystallography and molecular modelling.

Authors:  G M Clore; A M Gronenborn; G Carlson; E F Meyer
Journal:  J Mol Biol       Date:  1986-07-20       Impact factor: 5.469

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