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Experimental Validation of Bacillus anthracis A16R Proteogenomics
Anthrax, caused by the pathogenic bacterium Bacillus anthracis, is a zoonosis that causes serious disease and is of significant concern as a biological warfare agent. Validating annotated genes and reannotating misannotated genes are important to understand its biology and mechanisms of pathogenicit...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589699/ https://www.ncbi.nlm.nih.gov/pubmed/26423727 http://dx.doi.org/10.1038/srep14608 |
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author | Gao, Zhiqi Wang, Zhiqiang Zhang, Kun Li, Yanchang Zhang, Tao Wang, Dongshu Liu, Xiankai Feng, Erling Chang, Lei Xu, Junjie He, Simin Xu, Ping Zhu, Li Wang, Hengliang |
author_facet | Gao, Zhiqi Wang, Zhiqiang Zhang, Kun Li, Yanchang Zhang, Tao Wang, Dongshu Liu, Xiankai Feng, Erling Chang, Lei Xu, Junjie He, Simin Xu, Ping Zhu, Li Wang, Hengliang |
author_sort | Gao, Zhiqi |
collection | PubMed |
description | Anthrax, caused by the pathogenic bacterium Bacillus anthracis, is a zoonosis that causes serious disease and is of significant concern as a biological warfare agent. Validating annotated genes and reannotating misannotated genes are important to understand its biology and mechanisms of pathogenicity. Proteomics studies are, to date, the best method for verifying and improving current annotations. To this end, the proteome of B. anthracis A16R was analyzed via one-dimensional gel electrophoresis followed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). In total, we identified 3,712 proteins, including many regulatory and key functional proteins at relatively low abundance, representing the most complete proteome of B. anthracis to date. Interestingly, eight sequencing errors were detected by proteogenomic analysis and corrected by resequencing. More importantly, three unannotated peptide fragments were identified in this study and validated by synthetic peptide mass spectrum mapping and green fluorescent protein fusion experiments. These data not only give a more comprehensive understanding of B. anthracis A16R but also demonstrate the power of proteomics to improve genome annotations and determine true translational elements. |
format | Online Article Text |
id | pubmed-4589699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45896992015-10-13 Experimental Validation of Bacillus anthracis A16R Proteogenomics Gao, Zhiqi Wang, Zhiqiang Zhang, Kun Li, Yanchang Zhang, Tao Wang, Dongshu Liu, Xiankai Feng, Erling Chang, Lei Xu, Junjie He, Simin Xu, Ping Zhu, Li Wang, Hengliang Sci Rep Article Anthrax, caused by the pathogenic bacterium Bacillus anthracis, is a zoonosis that causes serious disease and is of significant concern as a biological warfare agent. Validating annotated genes and reannotating misannotated genes are important to understand its biology and mechanisms of pathogenicity. Proteomics studies are, to date, the best method for verifying and improving current annotations. To this end, the proteome of B. anthracis A16R was analyzed via one-dimensional gel electrophoresis followed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). In total, we identified 3,712 proteins, including many regulatory and key functional proteins at relatively low abundance, representing the most complete proteome of B. anthracis to date. Interestingly, eight sequencing errors were detected by proteogenomic analysis and corrected by resequencing. More importantly, three unannotated peptide fragments were identified in this study and validated by synthetic peptide mass spectrum mapping and green fluorescent protein fusion experiments. These data not only give a more comprehensive understanding of B. anthracis A16R but also demonstrate the power of proteomics to improve genome annotations and determine true translational elements. Nature Publishing Group 2015-10-01 /pmc/articles/PMC4589699/ /pubmed/26423727 http://dx.doi.org/10.1038/srep14608 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gao, Zhiqi Wang, Zhiqiang Zhang, Kun Li, Yanchang Zhang, Tao Wang, Dongshu Liu, Xiankai Feng, Erling Chang, Lei Xu, Junjie He, Simin Xu, Ping Zhu, Li Wang, Hengliang Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title | Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title_full | Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title_fullStr | Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title_full_unstemmed | Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title_short | Experimental Validation of Bacillus anthracis A16R Proteogenomics |
title_sort | experimental validation of bacillus anthracis a16r proteogenomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589699/ https://www.ncbi.nlm.nih.gov/pubmed/26423727 http://dx.doi.org/10.1038/srep14608 |
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