Paper detail

Polarization effect of zinc on the region 1-16 of amyloid-beta peptide: a molecular dynamics study

Zinc is found saturated in the deposited Amyloid-beta (AB) peptide plaques in brains of patients subjected to Alzheimer disease (AD). Zinc binding to AB promotes aggregations, including the toxic soluble AB species. Up to now, only the region 1-16 of AB complexed with Zinc (AB16-Zn) is defined structurally in experiment, requiring an efficient theoretical method to present the interaction between zinc and AB peptide. In order to explore the induced polarization effect on the global conformation fluctuations and the experimentally observed coordination mode of AB16-Zn, in this work we consider an all-atom molecular dynamics (MD) of AB16-Zn solvated in implicit water. In our model the polarization effect affects the whole peptide is applied. The induced dipoles are divided into three distinct scales according to their distances from zinc. Besides, the atomistic polarizability on the coordinating sidechains is rescaled to describe the electron redistribution effect. As a comparison, another model which exactly follows the method of Sakharov and Lim (J. Am. Chem. Soc., 127, 13, 2005) has been discussed also. We show that, associated with proper van der Waals (vdW) parameters, our model not only obtains the reasonable coordinating configuration of zinc binding site, but also retains the global stabilization, especially the N-terminal region, of the AB16-Zn. We suggest that it is the induced polarization effect that promotes reasonable solvent exposures of hydrophobic/hydrophilic residues regarding zinc-induced AB aggregation.