Year: 2023
Type: article
Abstract: The periplasmic chaperone SilF has been identified as part of an Ag(I) detoxification system in Gram-negative bacteria. Sil proteins also bind Cu(I) but with reported weaker affinity, therefore leading to the designation of a specific detoxification system for Ag(I). Using isothermal titration calorimetry, we show that binding of both ions is not only tighter than previously thought but of very similar affinities. We investigated the structural origins of ion binding using molecular dynamics and QM/MM simulations underpinned by structural and biophysical experiments. The results of this analysis showed that the binding site adapts to accommodate either ion, with key interactions with the solvent in the case of Cu(I). The implications of this are that Gram-negative bacteria do not appear to have evolved a specific Ag(I) efflux system but take advantage of the existing Cu(I) detoxification system. Therefore, there are consequences for how we define a particular metal resistance mechanism and understand its evolution in the environment.
Source: Journal of Biological Chemistry
Language: English
Topic: Heat shock proteins research
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,800
Awards: Dynamic Structural Biology: New Tools and Strategies for General Applications, G3168370783, A laboratory for membrane protein structural biology, 17ALERT bid: A new multi-wavelength analytical ultracentrifuge for the study of biomolecular interactions, Nottingham-Rothamsted Doctoral Training Partnership, G5542397878, G7245746529, G8212379191
OpenAlex ID: W4387564516
