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AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides

BACKGROUND: Protein aggregation correlates with the development of several debilitating human disorders of growing incidence, such as Alzheimer's and Parkinson's diseases. On the biotechnological side, protein production is often hampered by the accumulation of recombinant proteins into ag...

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Autores principales: Conchillo-Solé, Oscar, de Groot, Natalia S, Avilés, Francesc X, Vendrell, Josep, Daura, Xavier, Ventura, Salvador
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828741/
https://www.ncbi.nlm.nih.gov/pubmed/17324296
http://dx.doi.org/10.1186/1471-2105-8-65
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author Conchillo-Solé, Oscar
de Groot, Natalia S
Avilés, Francesc X
Vendrell, Josep
Daura, Xavier
Ventura, Salvador
author_facet Conchillo-Solé, Oscar
de Groot, Natalia S
Avilés, Francesc X
Vendrell, Josep
Daura, Xavier
Ventura, Salvador
author_sort Conchillo-Solé, Oscar
collection PubMed
description BACKGROUND: Protein aggregation correlates with the development of several debilitating human disorders of growing incidence, such as Alzheimer's and Parkinson's diseases. On the biotechnological side, protein production is often hampered by the accumulation of recombinant proteins into aggregates. Thus, the development of methods to anticipate the aggregation properties of polypeptides is receiving increasing attention. AGGRESCAN is a web-based software for the prediction of aggregation-prone segments in protein sequences, the analysis of the effect of mutations on protein aggregation propensities and the comparison of the aggregation properties of different proteins or protein sets. RESULTS: AGGRESCAN is based on an aggregation-propensity scale for natural amino acids derived from in vivo experiments and on the assumption that short and specific sequence stretches modulate protein aggregation. The algorithm is shown to identify a series of protein fragments involved in the aggregation of disease-related proteins and to predict the effect of genetic mutations on their deposition propensities. It also provides new insights into the differential aggregation properties displayed by globular proteins, natively unfolded polypeptides, amyloidogenic proteins and proteins found in bacterial inclusion bodies. CONCLUSION: By identifying aggregation-prone segments in proteins, AGGRESCAN shall facilitate (i) the identification of possible therapeutic targets for anti-depositional strategies in conformational diseases and (ii) the anticipation of aggregation phenomena during storage or recombinant production of bioactive polypeptides or polypeptide sets.
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spelling pubmed-18287412007-03-20 AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides Conchillo-Solé, Oscar de Groot, Natalia S Avilés, Francesc X Vendrell, Josep Daura, Xavier Ventura, Salvador BMC Bioinformatics Software BACKGROUND: Protein aggregation correlates with the development of several debilitating human disorders of growing incidence, such as Alzheimer's and Parkinson's diseases. On the biotechnological side, protein production is often hampered by the accumulation of recombinant proteins into aggregates. Thus, the development of methods to anticipate the aggregation properties of polypeptides is receiving increasing attention. AGGRESCAN is a web-based software for the prediction of aggregation-prone segments in protein sequences, the analysis of the effect of mutations on protein aggregation propensities and the comparison of the aggregation properties of different proteins or protein sets. RESULTS: AGGRESCAN is based on an aggregation-propensity scale for natural amino acids derived from in vivo experiments and on the assumption that short and specific sequence stretches modulate protein aggregation. The algorithm is shown to identify a series of protein fragments involved in the aggregation of disease-related proteins and to predict the effect of genetic mutations on their deposition propensities. It also provides new insights into the differential aggregation properties displayed by globular proteins, natively unfolded polypeptides, amyloidogenic proteins and proteins found in bacterial inclusion bodies. CONCLUSION: By identifying aggregation-prone segments in proteins, AGGRESCAN shall facilitate (i) the identification of possible therapeutic targets for anti-depositional strategies in conformational diseases and (ii) the anticipation of aggregation phenomena during storage or recombinant production of bioactive polypeptides or polypeptide sets. BioMed Central 2007-02-27 /pmc/articles/PMC1828741/ /pubmed/17324296 http://dx.doi.org/10.1186/1471-2105-8-65 Text en Copyright © 2007 Conchillo-Solé et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Conchillo-Solé, Oscar
de Groot, Natalia S
Avilés, Francesc X
Vendrell, Josep
Daura, Xavier
Ventura, Salvador
AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title_full AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title_fullStr AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title_full_unstemmed AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title_short AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
title_sort aggrescan: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828741/
https://www.ncbi.nlm.nih.gov/pubmed/17324296
http://dx.doi.org/10.1186/1471-2105-8-65
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