Literature DB >> 6627097

An optical stopped-flow and 1H and 113Cd nuclear magnetic resonance study of the kinetics and stoichiometry of the interaction of the lanthanide Yb3+ with carp parvalbumin.

D C Corson, L Lee, G A McQuaid, B D Sykes.   

Abstract

The rate constants for the dissociation of the lanthanide Yb3+ from the CD and EF calcium-binding sites of carp parvalbumin (isoelectric point, 4.25) have been measured using optical stopped-flow and 1H nuclear magnetic resonance (NMR) methods. The off-rate constants for Yb3+ are 1.5 X 10(-1) and 1.3 X 10(-3) s-1, respectively, at pH 6.6 and 23 degrees C. The relative displacement of Ca2+ from the two sites by Yb3+ was determined from the observed amplitude of the fast and slow kinetic phases. Yb3+-shifted 1H-NMR spectra of parvalbumin are presented as a function of pH, concentration, and H2O:D2O ratio to relate the NMR results to the kinetic and optical results. The displacement of Cd2+ from parvalbumin by Yb3+ was studied using 113Cd NMR. All of the results show the sequential displacement of Ca2+ from the CD and EF sites of parvalbumin by Yb3+. Some results are also presented for Tb3+ and Gd3+.

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Year:  1983        PMID: 6627097     DOI: 10.1139/o83-110

Source DB:  PubMed          Journal:  Can J Biochem Cell Biol        ISSN: 0714-7511


  3 in total

1.  Structural studies of calcium-binding proteins using nuclear magnetic resonance.

Authors:  L Lee; D C Corson; B D Sykes
Journal:  Biophys J       Date:  1985-02       Impact factor: 4.033

2.  Metal-ion binding to parvalbumin. A 113Cd-n.m.r. study of the binding of different lanthanide ions.

Authors:  T Drakenberg; M Swärd; A Cavé; J Parello
Journal:  Biochem J       Date:  1985-05-01       Impact factor: 3.857

3.  An NMR method for studying the kinetics of metal exchange in biomolecular systems.

Authors:  Renato Barbieri; P J Hore; Claudio Luchina; Roberta Pierattelli
Journal:  J Biomol NMR       Date:  2002-08       Impact factor: 2.835

  3 in total

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