Role of Water in Mediating the Assembly of Alzheimer Amyloid-β Aβ16−22 Protofilaments

Citations Over TimeTop 10% of 2008 papers

Abstract

The role of water in promoting the formation of protofilaments (the basic building blocks of amyloid fibrils) is investigated using fully atomic molecular dynamics simulations. Our model protofilament consists of two parallel beta-sheets of Alzheimer Amyloid-beta 16-22 peptides (Ac-K(16)-L(17)-V(18)-F(19)-F(20)-A(21)-E(22)-NH2). Each sheet presents a distinct hydrophobic and hydrophilic face and together self-assemble to a stable protofilament with a core consisting of purely hydrophobic residues (L(17), F(19), A(21)), with the two charged residues (K(16), E(22)) pointing to the solvent. Our simulations reveal a subtle interplay between a water mediated assembly and one driven by favorable energetic interactions between specific residues forming the interior of the protofilament. A dewetting transition, in which water expulsion precedes hydrophobic collapse, is observed for some, but not all molecular dynamics trajectories. In the trajectories in which no dewetting is observed, water expulsion and hydrophobic collapse occur simultaneously, with protofilament assembly driven by direct interactions between the hydrophobic side chains of the peptides (particularly between F-F residues). For those same trajectories, a small increase in the temperature of the simulation (on the order of 20 K) or a modest reduction in the peptide-water van der Waals attraction (on the order of 10%) is sufficient to induce a dewetting transition, suggesting that the existence of a dewetting transition in simulation might be sensitive to the details of the force field parametrization.

Related Papers

• → Hydrophobic Interactions and Dewetting between Plates with Hydrophobic and Hydrophilic Domains(2009)117 cited
• → Inversion of the Balance between Hydrophobic and Hydrogen Bonding Interactions in Protein Folding and Aggregation(2011)114 cited
• → Fluctuation-induced forces governed by the dielectric properties of water—A contribution to the hydrophobic interaction(2015)14 cited
• → Hydrophobic Interactions and Dewetting between Plates with Hydrophobic and Hydrophilic Domains(2008)4 cited
• Effects of Electrostatic and Hydrophobic Interaction on the Stability of SARS Coronavirus 3CL Proteinase Dimer(2005)