Interactions between proteins and metal cations are central to biochemical processes and shape protein structures. SilE, an intrinsically disordered protein involved in bacterial silver-resistance, folds into α-helices upon binding Ag+ ions. Focusing on the B1 peptide fragment from SilE, we investigate the mechanism of Ag+-induced folding with atomistic simulations and experiments. Guided by Mass Spectrometry and NMR, we prepare a structural model of Ag+-bound B1, which we parametrize using DFT. Then, with replica-exchange simulations and deep learning, we map B1’s folding landscape and how it is shaped by Ag+. Specifically, Ag+ binding promotes folding by lowering the entropy of the disordered state and stabilizing the folded state. We also describe how Ag+ alters the folding pathways. Overall, we improve the understanding of metal-induced protein folding and lay the groundwork for further computational investigations of the bacterial silver-resistance machinery.
Blanc et al. (Tue,) studied this question.