An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data

<p>Abstract</p> <p>Background</p> <p>The ecological niche occupied by a fungal species, its pathogenicity and its usefulness as a microbial cell factory to a large degree depends on its secretome. Protein secretion usually requires the presence of a N-terminal signal pe...

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Main Authors: Martens-Uzunova Elena S, Braaksma Machtelt, Punt Peter J, Schaap Peter J
Format: Article
Language:English
Published: BMC 2010-10-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/11/584
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spelling doaj-3830092b0fe8460aa8749e70680557152020-11-24T23:08:01ZengBMCBMC Genomics1471-21642010-10-0111158410.1186/1471-2164-11-584An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics dataMartens-Uzunova Elena SBraaksma MachteltPunt Peter JSchaap Peter J<p>Abstract</p> <p>Background</p> <p>The ecological niche occupied by a fungal species, its pathogenicity and its usefulness as a microbial cell factory to a large degree depends on its secretome. Protein secretion usually requires the presence of a N-terminal signal peptide (SP) and by scanning for this feature using available highly accurate SP-prediction tools, the fraction of potentially secreted proteins can be directly predicted. However, prediction of a SP does not guarantee that the protein is actually secreted and current <it>in silico </it>prediction methods suffer from gene-model errors introduced during genome annotation.</p> <p>Results</p> <p>A majority rule based classifier that also evaluates signal peptide predictions from the best homologs of three neighbouring <it>Aspergillus </it>species was developed to create an improved list of potential signal peptide containing proteins encoded by the <it>Aspergillus niger </it>genome. As a complement to these <it>in silico </it>predictions, the secretome associated with growth and upon carbon source depletion was determined using a shotgun proteomics approach. Overall, some 200 proteins with a predicted signal peptide were identified to be secreted proteins. Concordant changes in the secretome state were observed as a response to changes in growth/culture conditions. Additionally, two proteins secreted via a non-classical route operating in <it>A. niger </it>were identified.</p> <p>Conclusions</p> <p>We were able to improve the <it>in silico </it>inventory of <it>A. niger </it>secretory proteins by combining different gene-model predictions from neighbouring Aspergilli and thereby avoiding prediction conflicts associated with inaccurate gene-models. The expected accuracy of signal peptide prediction for proteins that lack homologous sequences in the proteomes of related species is 85%. An experimental validation of the predicted proteome confirmed <it>in silico </it>predictions.</p> http://www.biomedcentral.com/1471-2164/11/584
collection DOAJ
language English
format Article
sources DOAJ
author Martens-Uzunova Elena S
Braaksma Machtelt
Punt Peter J
Schaap Peter J
spellingShingle Martens-Uzunova Elena S
Braaksma Machtelt
Punt Peter J
Schaap Peter J
An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
BMC Genomics
author_facet Martens-Uzunova Elena S
Braaksma Machtelt
Punt Peter J
Schaap Peter J
author_sort Martens-Uzunova Elena S
title An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
title_short An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
title_full An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
title_fullStr An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
title_full_unstemmed An inventory of the <it>Aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
title_sort inventory of the <it>aspergillus niger </it>secretome by combining <it>in silico </it>predictions with shotgun proteomics data
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2010-10-01
description <p>Abstract</p> <p>Background</p> <p>The ecological niche occupied by a fungal species, its pathogenicity and its usefulness as a microbial cell factory to a large degree depends on its secretome. Protein secretion usually requires the presence of a N-terminal signal peptide (SP) and by scanning for this feature using available highly accurate SP-prediction tools, the fraction of potentially secreted proteins can be directly predicted. However, prediction of a SP does not guarantee that the protein is actually secreted and current <it>in silico </it>prediction methods suffer from gene-model errors introduced during genome annotation.</p> <p>Results</p> <p>A majority rule based classifier that also evaluates signal peptide predictions from the best homologs of three neighbouring <it>Aspergillus </it>species was developed to create an improved list of potential signal peptide containing proteins encoded by the <it>Aspergillus niger </it>genome. As a complement to these <it>in silico </it>predictions, the secretome associated with growth and upon carbon source depletion was determined using a shotgun proteomics approach. Overall, some 200 proteins with a predicted signal peptide were identified to be secreted proteins. Concordant changes in the secretome state were observed as a response to changes in growth/culture conditions. Additionally, two proteins secreted via a non-classical route operating in <it>A. niger </it>were identified.</p> <p>Conclusions</p> <p>We were able to improve the <it>in silico </it>inventory of <it>A. niger </it>secretory proteins by combining different gene-model predictions from neighbouring Aspergilli and thereby avoiding prediction conflicts associated with inaccurate gene-models. The expected accuracy of signal peptide prediction for proteins that lack homologous sequences in the proteomes of related species is 85%. An experimental validation of the predicted proteome confirmed <it>in silico </it>predictions.</p>
url http://www.biomedcentral.com/1471-2164/11/584
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