@article {2016|1703,
	title = {Lattice model for amyloid peptides: OPEP force field parametrization and applications to the nucleus size of Alzheimer{\textquoteright}s peptides},
	journal = {J. Chem. Phys.},
	volume = {144},
	number = {20},
	year = {2016},
	month = {may},
	abstract = {Coarse-grained protein lattice models approximate atomistic details and keep the essential interactions. They are, therefore, suitable for capturing generic features of protein folding and amyloid formation at low computational cost. As our aim is to study the critical nucleus sizes of two experimentally well-characterized peptide fragments A beta(16-22) and A beta(37-42) of the full length A beta(1-42) Alzheimer{\textquoteright}s peptide, it is important that simulations with the lattice model reproduce all-atom simulations. In this study, we present a comprehensive force field parameterization based on the OPEP (Optimized Potential for Efficient protein structure Prediction) force field for an on-lattice protein model, which incorporates explicitly the formation of hydrogen bonds and directions of side-chains. Our bottom-up approach starts with the determination of the best lattice force parameters for the A beta(16-22) dimer by fitting its equilibrium parallel and anti-parallel beta-sheet populations to all-atom simulation results. Surprisingly, the calibrated force field is transferable to the trimer of A beta(16-22) and the dimer and trimer of A beta(37-42). Encouraged by this finding, we characterized the free energy landscapes of the two decamers. The dominant structure of the A beta(16-22) decamer matches the microcrystal structure. Pushing the simulations for aggregates between 4-mer and 12-mer suggests a nucleus size for fibril formation of 10 chains. In contrast, the A beta(37-42) decamer is largely disordered with mixed by parallel and antiparallel chains, suggesting that the nucleus size is >10 peptides. Our refined force field coupled to this on-lattice model should provide useful insights into the critical nucleation number associated with neurodegenerative diseases. Published by AIP Publishing.},
	issn = {0021-9606},
	doi = {10.1063/1.4951739},
	author = {Thanh-Thuy Tran and Phuong Hoang Nguyen and Philippe Derreumaux}
}
@article {2010|1885,
	title = {Low molecular weight oligomers of amyloid peptides display beta-barrel conformations: A replica exchange molecular dynamics study in explicit solvent},
	journal = {J. Chem. Phys.},
	volume = {132},
	number = {16},
	year = {2010},
	month = {apr},
	pages = {165103},
	doi = {10.1063/1.3385470},
	author = {De Simone, Alfonso and Philippe Derreumaux}
}
@article {1998|1624,
	title = {The loop opening/closing motion of the enzyme triosephosphate isomerase},
	journal = {Biophys. J.},
	volume = {74},
	number = {1},
	year = {1998},
	month = {jan},
	pages = {72{\textendash}81},
	author = {Philippe Derreumaux and Schlick, T.}
}
@article {1995|1988,
	title = {LONG TIMESTEP DYNAMICS OF PEPTIDES BY THE DYNAMICS DRIVER APPROACH},
	journal = {Proteins-structure Function and Genetics},
	volume = {21},
	number = {4},
	year = {1995},
	month = {apr},
	pages = {282{\textendash}302},
	doi = {10.1002/prot.340210403},
	author = {Philippe Derreumaux and SCHLICK, T}
}
