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BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis

Amyloids and prion proteins are clinically and biologically important β-structures, whose supersecondary structures are difficult to determine by standard experimental or computational means. In addition, significant conformational heterogeneity is known or suspected to exist in many amyloid fibrils...

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Detalles Bibliográficos
Autores principales: Bryan, Allen W., Menke, Matthew, Cowen, Lenore J., Lindquist, Susan L., Berger, Bonnie
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2653728/
https://www.ncbi.nlm.nih.gov/pubmed/19325876
http://dx.doi.org/10.1371/journal.pcbi.1000333
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author Bryan, Allen W.
Menke, Matthew
Cowen, Lenore J.
Lindquist, Susan L.
Berger, Bonnie
author_facet Bryan, Allen W.
Menke, Matthew
Cowen, Lenore J.
Lindquist, Susan L.
Berger, Bonnie
author_sort Bryan, Allen W.
collection PubMed
description Amyloids and prion proteins are clinically and biologically important β-structures, whose supersecondary structures are difficult to determine by standard experimental or computational means. In addition, significant conformational heterogeneity is known or suspected to exist in many amyloid fibrils. Recent work has indicated the utility of pairwise probabilistic statistics in β-structure prediction. We develop here a new strategy for β-structure prediction, emphasizing the determination of β-strands and pairs of β-strands as fundamental units of β-structure. Our program, BETASCAN, calculates likelihood scores for potential β-strands and strand-pairs based on correlations observed in parallel β-sheets. The program then determines the strands and pairs with the greatest local likelihood for all of the sequence's potential β-structures. BETASCAN suggests multiple alternate folding patterns and assigns relative a priori probabilities based solely on amino acid sequence, probability tables, and pre-chosen parameters. The algorithm compares favorably with the results of previous algorithms (BETAPRO, PASTA, SALSA, TANGO, and Zyggregator) in β-structure prediction and amyloid propensity prediction. Accurate prediction is demonstrated for experimentally determined amyloid β-structures, for a set of known β-aggregates, and for the parallel β-strands of β-helices, amyloid-like globular proteins. BETASCAN is able both to detect β-strands with higher sensitivity and to detect the edges of β-strands in a richly β-like sequence. For two proteins (Aβ and Het-s), there exist multiple sets of experimental data implying contradictory structures; BETASCAN is able to detect each competing structure as a potential structure variant. The ability to correlate multiple alternate β-structures to experiment opens the possibility of computational investigation of prion strains and structural heterogeneity of amyloid. BETASCAN is publicly accessible on the Web at http://betascan.csail.mit.edu.
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spelling pubmed-26537282009-03-27 BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis Bryan, Allen W. Menke, Matthew Cowen, Lenore J. Lindquist, Susan L. Berger, Bonnie PLoS Comput Biol Research Article Amyloids and prion proteins are clinically and biologically important β-structures, whose supersecondary structures are difficult to determine by standard experimental or computational means. In addition, significant conformational heterogeneity is known or suspected to exist in many amyloid fibrils. Recent work has indicated the utility of pairwise probabilistic statistics in β-structure prediction. We develop here a new strategy for β-structure prediction, emphasizing the determination of β-strands and pairs of β-strands as fundamental units of β-structure. Our program, BETASCAN, calculates likelihood scores for potential β-strands and strand-pairs based on correlations observed in parallel β-sheets. The program then determines the strands and pairs with the greatest local likelihood for all of the sequence's potential β-structures. BETASCAN suggests multiple alternate folding patterns and assigns relative a priori probabilities based solely on amino acid sequence, probability tables, and pre-chosen parameters. The algorithm compares favorably with the results of previous algorithms (BETAPRO, PASTA, SALSA, TANGO, and Zyggregator) in β-structure prediction and amyloid propensity prediction. Accurate prediction is demonstrated for experimentally determined amyloid β-structures, for a set of known β-aggregates, and for the parallel β-strands of β-helices, amyloid-like globular proteins. BETASCAN is able both to detect β-strands with higher sensitivity and to detect the edges of β-strands in a richly β-like sequence. For two proteins (Aβ and Het-s), there exist multiple sets of experimental data implying contradictory structures; BETASCAN is able to detect each competing structure as a potential structure variant. The ability to correlate multiple alternate β-structures to experiment opens the possibility of computational investigation of prion strains and structural heterogeneity of amyloid. BETASCAN is publicly accessible on the Web at http://betascan.csail.mit.edu. Public Library of Science 2009-03-27 /pmc/articles/PMC2653728/ /pubmed/19325876 http://dx.doi.org/10.1371/journal.pcbi.1000333 Text en Bryan, Jr. et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bryan, Allen W.
Menke, Matthew
Cowen, Lenore J.
Lindquist, Susan L.
Berger, Bonnie
BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title_full BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title_fullStr BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title_full_unstemmed BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title_short BETASCAN: Probable β-amyloids Identified by Pairwise Probabilistic Analysis
title_sort betascan: probable β-amyloids identified by pairwise probabilistic analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2653728/
https://www.ncbi.nlm.nih.gov/pubmed/19325876
http://dx.doi.org/10.1371/journal.pcbi.1000333
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