Publication Date:
2019
abstract:
Ions have an essential role in many biological processes. In particular when the
charge density is high (Mg, Ca, Zn) and when charge changes according to microenvironmental
conditions (Fe, Cu, Mn). Metal ions often interact with disordered proteins, with effects yet to be
understood. The affinity is high enough to compete with structured proteins, but the structural and
catalytic activity of the metal center is often out of control and, therefore, potentially dangerous
for cells.
In this contribution, I shall summarize this role with models applied to two examples involving
intrinsically disordered proteins. In the first example, we investigate the interactions between
osteopontin and nucleic acids [1], describing the role of Mg in modulating protein association. In
the second example, we apply a high-throughput modelling of Cu-amyloid beta complex in
contact with dioxygen, with the aim at providing a tool to dissect the structural features that
characterize dangerous catalysts in neurodegeneration [2,3]. The latter is a paradigmatic example
where the oxidative pathway induced by sporadic copper catalysts triggers cell death.
Iris type:
04.02 Abstract in Atti di convegno
Keywords:
Intrinsically disordered proteins; metal ions
List of contributors: