On the reactivity of metallothioneins with 5,5'-dithiobis-(2-nitrobenzoic acid)

Biochem J. 1981 Feb 1;193(2):441-6. doi: 10.1042/bj1930441.

Abstract

Rat liver and horse kidney metallothioneins react with 5,5'-dithiobis-(2-nitrobenzoic acid) (Nbs2) to release 5-thio-2-nitrobenzoate and metal ions. The reactions are slow and exhibit biphasic kinetics with each process having an empirical rate law of the form: rate - k[RSM] X [Nbs2] + k'[RSM], where RSM represents mental-bound thiolate groups. The pseudo-first-order rates are insensitive to pH but are modified in guanidine hydrochloride solution. Rat liver metallothioneins of variable zinc, copper and cadmium composition react similarly and give observable thiol/total metal ratios in good agreement with stoichiometries of SH/(Cd + Zn) of 3 and SH/Cu of 1. A model complex cadmium-2,3-dimercaptopropanol, resembles the proteins in its reaction with Nbs2.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Binding Sites
  • Dimercaprol / metabolism
  • Dithionitrobenzoic Acid / metabolism*
  • Horses
  • Hydrogen-Ion Concentration
  • Kidney / metabolism
  • Kinetics
  • Liver / metabolism
  • Metalloproteins / metabolism*
  • Metallothionein / metabolism*
  • Nitrobenzoates / metabolism*
  • Rats

Substances

  • Metalloproteins
  • Nitrobenzoates
  • Dimercaprol
  • Metallothionein
  • Dithionitrobenzoic Acid