Folding and stability of the three‐stranded β‐sheet peptide Betanova: Insights from molecular dynamics simulations

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Abstract
The dynamics of the three‐stranded β‐sheet peptide Betanova has been studied at four different temperatures (280, 300, 350, and 450 K by molecular dynamics simulation techniques, in explicit water. Two 20‐ns simulations at 280 K indicate that the peptide remains very flexible under “folding” conditions sampling a range of conformations that together satisfy the nuclear magnetic resonance (NMR)‐derived experimental constraints. Two simulations at 300 K (above the experimental folding temperature) of 20 ns each show partial formation of “native”‐like structure, which also satisfies most of the NOE constraints at 280 K. At higher temperature, the presence of compact states, in which a series of hydrophobic contacts remain present, are observed. This is consistent with experimental observations regarding the role of hydrophobic contacts in determining the peptide's stability and in initiating the formation of turns and loops. A set of different structures is shown to satisfy NMR‐derived distance restraints and a possible mechanism for the folding of the peptide into the NMR‐determined structure is proposed. Proteins 2002;46:380–392.