A metal-trap tests and refines blueprints to engineer cellular protein metalation with different elements.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39827241.
- Also identified by DOI 10.1038/s41467-025-56199-w and PMC identifier 11742986.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
It has been challenging to test how proteins acquire specific metals in cells. The speciation of metalation is thought to depend on the preferences of proteins for different metals competing at intracellular metal-availabilities. This implies mis-metalation may occur if proteins become mis-matched to metal-availabilities in heterologous cells. Here we use a cyanobacterial Mn<sup>II</sup>-cupin (MncA) as a metal trap, to test predictions of metalation. By re-folding MncA in buffered competing metals, metal-preferences are determined. Relating metal-preferences to metal-availabilities estimated using cellular metal sensors, predicts mis-metalation of MncA with Fe<sup>II</sup> in E. coli. After expression in E. coli, predominantly Fe<sup>II</sup>-bound MncA is isolated experimentally. It is predicted that in metal-supplemented viable cells metal-MncA speciation should switch. Mn<sup>II</sup>-, Co<sup>II</sup>-, or Ni<sup>II</sup>-MncA are recovered from the respective metal-supplemented cells. Differences between observed and predicted metal-MncA speciation are used to refine estimated metal availabilities. Values are provided as blueprints to guide engineering biological protein metalation.
Medical subject headings
- Bacterial Proteins
- Azurin
- Metals
- Protein Engineering