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• W2087357689 abstract "Based on the crystal structure of the cross-β spine formed by the peptide NNQQNY, we have developed a computational approach for identifying those segments of amyloidogenic proteins that themselves can form amyloid-like fibrils. The approach builds on experiments showing that hexapeptides are sufficient for forming amyloid-like fibrils. Each six-residue peptide of a protein of interest is mapped onto an ensemble of templates, or 3D profile, generated from the crystal structure of the peptide NNQQNY by small displacements of one of the two intermeshed β-sheets relative to the other. The energy of each mapping of a sequence to the profile is evaluated by using rosettadesign , and the lowest energy match for a given peptide to the template library is taken as the putative prediction. If the energy of the putative prediction is lower than a threshold value, a prediction of fibril formation is made. This method can reach an accuracy of ≈80% with a P value of ≈10 −12 when a conservative energy threshold is used to separate peptides that form fibrils from those that do not. We see enrichment for positive predictions in a set of fibril-forming segments of amyloid proteins, and we illustrate the method with applications to proteins of interest in amyloid research." @default.
• W2087357689 created "2016-06-24" @default.
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• W2087357689 date "2006-03-07" @default.
• W2087357689 modified "2023-10-10" @default.
• W2087357689 title "The 3D profile method for identifying fibril-forming segments of proteins" @default.
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• W2087357689 doi "https://doi.org/10.1073/pnas.0511295103" @default.
• W2087357689 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1449648" @default.
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