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In Silico Classification of Proteins from Acidic and Neutral Cytoplasms

Protein acidostability is a common problem in biopharmaceutical and other industries. However, it remains a great challenge to engineer proteins for enhanced acidostability because our knowledge of protein acidostabilization is still very limited. In this paper, we present a comparative study of pro...

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Detalles Bibliográficos
Autores principales: Fang, Yaping, Middaugh, C. Russell, Fang, Jianwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458925/
https://www.ncbi.nlm.nih.gov/pubmed/23049817
http://dx.doi.org/10.1371/journal.pone.0045585
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author Fang, Yaping
Middaugh, C. Russell
Fang, Jianwen
author_facet Fang, Yaping
Middaugh, C. Russell
Fang, Jianwen
author_sort Fang, Yaping
collection PubMed
description Protein acidostability is a common problem in biopharmaceutical and other industries. However, it remains a great challenge to engineer proteins for enhanced acidostability because our knowledge of protein acidostabilization is still very limited. In this paper, we present a comparative study of proteins from bacteria with acidic (AP) and neutral cytoplasms (NP) using an integrated statistical and machine learning approach. We construct a set of 393 non-redundant AP-NP ortholog pairs and calculate a total of 889 sequence based features for these proteins. The pairwise alignments of these ortholog pairs are used to build a residue substitution propensity matrix between APs and NPs. We use Gini importance provided by the Random Forest algorithm to rank the relative importance of these features. A scoring function using the 10 most significant features is developed and optimized using a hill climbing algorithm. The accuracy of the score function is 86.01% in predicting AP-NP ortholog pairs and is 76.65% in predicting non-ortholog AP-NP pairs, suggesting that there are significant differences between APs and NPs which can be used to predict relative acidostability of proteins. The overall trends uncovered in the study can be used as general guidelines for designing acidostable proteins. To best of our knowledge, this work represents the first systematic comparative study of the acidostable proteins and their non-acidostable orthologs.
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spelling pubmed-34589252012-10-03 In Silico Classification of Proteins from Acidic and Neutral Cytoplasms Fang, Yaping Middaugh, C. Russell Fang, Jianwen PLoS One Research Article Protein acidostability is a common problem in biopharmaceutical and other industries. However, it remains a great challenge to engineer proteins for enhanced acidostability because our knowledge of protein acidostabilization is still very limited. In this paper, we present a comparative study of proteins from bacteria with acidic (AP) and neutral cytoplasms (NP) using an integrated statistical and machine learning approach. We construct a set of 393 non-redundant AP-NP ortholog pairs and calculate a total of 889 sequence based features for these proteins. The pairwise alignments of these ortholog pairs are used to build a residue substitution propensity matrix between APs and NPs. We use Gini importance provided by the Random Forest algorithm to rank the relative importance of these features. A scoring function using the 10 most significant features is developed and optimized using a hill climbing algorithm. The accuracy of the score function is 86.01% in predicting AP-NP ortholog pairs and is 76.65% in predicting non-ortholog AP-NP pairs, suggesting that there are significant differences between APs and NPs which can be used to predict relative acidostability of proteins. The overall trends uncovered in the study can be used as general guidelines for designing acidostable proteins. To best of our knowledge, this work represents the first systematic comparative study of the acidostable proteins and their non-acidostable orthologs. Public Library of Science 2012-09-26 /pmc/articles/PMC3458925/ /pubmed/23049817 http://dx.doi.org/10.1371/journal.pone.0045585 Text en © 2012 Fang 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
Fang, Yaping
Middaugh, C. Russell
Fang, Jianwen
In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title_full In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title_fullStr In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title_full_unstemmed In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title_short In Silico Classification of Proteins from Acidic and Neutral Cytoplasms
title_sort in silico classification of proteins from acidic and neutral cytoplasms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458925/
https://www.ncbi.nlm.nih.gov/pubmed/23049817
http://dx.doi.org/10.1371/journal.pone.0045585
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