Skip to Content
Merck
  • The histidine kinase CusS senses silver ions through direct binding by its sensor domain.

The histidine kinase CusS senses silver ions through direct binding by its sensor domain.

Biochimica et biophysica acta (2014-06-21)
Swapna A Gudipaty, Megan M McEvoy
ABSTRACT

The Cus system of Escherichia coli aids in protection of cells from high concentrations of Ag(I) and Cu(I). The histidine kinase CusS of the CusRS two-component system functions as a Ag(I)/Cu(I)-responsive sensor kinase and is essential for induction of the genes encoding the CusCFBA efflux pump. In this study, we have examined the molecular features of the sensor domain of CusS in order to understand how a metal-responsive histidine kinase senses specific metal ions. We find that the predicted periplasmic sensor domain of CusS directly interacts with Ag(I) ions and undergoes a conformational change upon metal binding. Metal binding also enhances the tendency of the domain to dimerize. These findings suggest a model for activation of the histidine kinase through metal binding events in the periplasmic sensor domain.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Copper, foil, thickness 1.0 mm, 99.999% trace metals basis
Sigma-Aldrich
Copper, wire, diam. 0.64 mm, 99.995% trace metals basis
Sigma-Aldrich
Copper, wire, diam. 1.0 mm, ≥99.9%
Sigma-Aldrich
Copper, wire, diam. 2.0 mm, 99.999% trace metals basis
Sigma-Aldrich
Silver, nanopowder, <150 nm particle size, 99% trace metals basis
Sigma-Aldrich
Silver, colloidal, 65-75% Ag basis
Sigma-Aldrich
Silver, nanopowder, <100 nm particle size, contains PVP as dispersant, 99.5% trace metals basis