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Table · dataset · 2017

Data for Ligand field molecular dynamics simulation of Pt(II)-phenanthroline binding to N-terminal fragment of amyloid-beta peptide

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We report microsecond timescale molecular dynamics simulation of the complex formed between Pt(II)-phenanthroline and the 16 N-terminal residues of the Aβ peptide that is implicated in the onset of Alzheimer’s disease, along with equivalent simulations of the metal-free peptide.

Description

Simulations from a variety of starting points reach equilibrium within 100 ns, as judged by root mean square deviation and radius of gyration.

Platinum-bound peptides deviate rather more from starting points, and adopt structures with larger radius of gyration, than their metal-free counterparts. Residues bound directly to Pt show smaller fluctuation, but others actually move more in the Pt-bound peptide. Hydrogen bonding within the peptide is disrupted by binding of Pt, whereas the presence of salt-bridges are enhanced.<br><br>Data record consists of a data archive file in .tar.gz format.

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DL_POLY Classic input and output files for 10 MD simulations: 5 of free peptide, 5 with Pt(phen).

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