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Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features

BACKGROUND: Ion mobility-mass spectrometry (IMMS), an analytical technique which combines the features of ion mobility spectrometry (IMS) and mass spectrometry (MS), can rapidly separates ions on a millisecond time-scale. IMMS becomes a powerful tool to analyzing complex mixtures, especially for the...

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Autores principales: Wang, Bing, Zhang, Jun, Chen, Peng, Ji, Zhiwei, Deng, Shuping, Li, Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654891/
https://www.ncbi.nlm.nih.gov/pubmed/23815343
http://dx.doi.org/10.1186/1471-2105-14-S8-S9
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author Wang, Bing
Zhang, Jun
Chen, Peng
Ji, Zhiwei
Deng, Shuping
Li, Chi
author_facet Wang, Bing
Zhang, Jun
Chen, Peng
Ji, Zhiwei
Deng, Shuping
Li, Chi
author_sort Wang, Bing
collection PubMed
description BACKGROUND: Ion mobility-mass spectrometry (IMMS), an analytical technique which combines the features of ion mobility spectrometry (IMS) and mass spectrometry (MS), can rapidly separates ions on a millisecond time-scale. IMMS becomes a powerful tool to analyzing complex mixtures, especially for the analysis of peptides in proteomics. The high-throughput nature of this technique provides a challenge for the identification of peptides in complex biological samples. As an important parameter, peptide drift time can be used for enhancing downstream data analysis in IMMS-based proteomics. RESULTS: In this paper, a model is presented based on least square support vectors regression (LS-SVR) method to predict peptide ion drift time in IMMS from the sequence-based features of peptide. Four descriptors were extracted from peptide sequence to represent peptide ions by a 34-component vector. The parameters of LS-SVR were selected by a grid searching strategy, and a 10-fold cross-validation approach was employed for the model training and testing. Our proposed method was tested on three datasets with different charge states. The high prediction performance achieve demonstrate the effectiveness and efficiency of the prediction model. CONCLUSIONS: Our proposed LS-SVR model can predict peptide drift time from sequence information in relative high prediction accuracy by a test on a dataset of 595 peptides. This work can enhance the confidence of protein identification by combining with current protein searching techniques.
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spelling pubmed-36548912013-05-20 Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features Wang, Bing Zhang, Jun Chen, Peng Ji, Zhiwei Deng, Shuping Li, Chi BMC Bioinformatics Proceedings BACKGROUND: Ion mobility-mass spectrometry (IMMS), an analytical technique which combines the features of ion mobility spectrometry (IMS) and mass spectrometry (MS), can rapidly separates ions on a millisecond time-scale. IMMS becomes a powerful tool to analyzing complex mixtures, especially for the analysis of peptides in proteomics. The high-throughput nature of this technique provides a challenge for the identification of peptides in complex biological samples. As an important parameter, peptide drift time can be used for enhancing downstream data analysis in IMMS-based proteomics. RESULTS: In this paper, a model is presented based on least square support vectors regression (LS-SVR) method to predict peptide ion drift time in IMMS from the sequence-based features of peptide. Four descriptors were extracted from peptide sequence to represent peptide ions by a 34-component vector. The parameters of LS-SVR were selected by a grid searching strategy, and a 10-fold cross-validation approach was employed for the model training and testing. Our proposed method was tested on three datasets with different charge states. The high prediction performance achieve demonstrate the effectiveness and efficiency of the prediction model. CONCLUSIONS: Our proposed LS-SVR model can predict peptide drift time from sequence information in relative high prediction accuracy by a test on a dataset of 595 peptides. This work can enhance the confidence of protein identification by combining with current protein searching techniques. BioMed Central 2013-05-09 /pmc/articles/PMC3654891/ /pubmed/23815343 http://dx.doi.org/10.1186/1471-2105-14-S8-S9 Text en Copyright © 2013 Wang 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 Proceedings
Wang, Bing
Zhang, Jun
Chen, Peng
Ji, Zhiwei
Deng, Shuping
Li, Chi
Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title_full Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title_fullStr Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title_full_unstemmed Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title_short Prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
title_sort prediction of peptide drift time in ion mobility mass spectrometry from sequence-based features
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654891/
https://www.ncbi.nlm.nih.gov/pubmed/23815343
http://dx.doi.org/10.1186/1471-2105-14-S8-S9
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