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Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors

Peptides are an important group of compounds contributing to the desired, as well as the undesired taste of a food product. Their taste impressions can include aspects of sweetness, bitterness, savoury, umami and many other impressions depending on the amino acids present as well as their sequence....

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Autores principales: Hollebrands, Boudewijn, Hageman, Jos A., van de Sande, Jasper W., Albada, Bauke, Janssen, Hans-Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185643/
https://www.ncbi.nlm.nih.gov/pubmed/37000211
http://dx.doi.org/10.1007/s00216-023-04670-2
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author Hollebrands, Boudewijn
Hageman, Jos A.
van de Sande, Jasper W.
Albada, Bauke
Janssen, Hans-Gerd
author_facet Hollebrands, Boudewijn
Hageman, Jos A.
van de Sande, Jasper W.
Albada, Bauke
Janssen, Hans-Gerd
author_sort Hollebrands, Boudewijn
collection PubMed
description Peptides are an important group of compounds contributing to the desired, as well as the undesired taste of a food product. Their taste impressions can include aspects of sweetness, bitterness, savoury, umami and many other impressions depending on the amino acids present as well as their sequence. Identification of short peptides in foods is challenging. We developed a method to assign identities to short peptides including homologous structures, i.e. peptides containing the same amino acids with a different sequence order, by accurate prediction of the retention times during reversed phase separation. To train the method, a large set of well-defined short peptides with systematic variations in the amino acid sequence was prepared by a novel synthesis strategy called ‘swapped-sequence synthesis’. Additionally, several proteins were enzymatically digested to yield short peptides. Experimental retention times were determined after reversed phase separation and peptide MS(2) data was acquired using a high-resolution mass spectrometer operated in data-dependent acquisition mode (DDA). A support vector regression model was trained using a combination of existing sequence-independent peptide descriptors and a newly derived set of selected amino acid index derived sequence-specific peptide (ASP) descriptors. The model was trained and validated using the experimental retention times of the 713 small food-relevant peptides prepared. Whilst selecting the most useful ASP descriptors for our model, special attention was given to predict the retention time differences between homologous peptide structures. Inclusion of ASP descriptors greatly improved the ability to accurately predict retention times, including retention time differences between 157 homologous peptide pairs. The final prediction model had a goodness-of-fit (Q(2)) of 0.94; moreover for 93% of the short peptides, the elution order was correctly predicted. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04670-2.
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spelling pubmed-101856432023-05-17 Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors Hollebrands, Boudewijn Hageman, Jos A. van de Sande, Jasper W. Albada, Bauke Janssen, Hans-Gerd Anal Bioanal Chem Research Paper Peptides are an important group of compounds contributing to the desired, as well as the undesired taste of a food product. Their taste impressions can include aspects of sweetness, bitterness, savoury, umami and many other impressions depending on the amino acids present as well as their sequence. Identification of short peptides in foods is challenging. We developed a method to assign identities to short peptides including homologous structures, i.e. peptides containing the same amino acids with a different sequence order, by accurate prediction of the retention times during reversed phase separation. To train the method, a large set of well-defined short peptides with systematic variations in the amino acid sequence was prepared by a novel synthesis strategy called ‘swapped-sequence synthesis’. Additionally, several proteins were enzymatically digested to yield short peptides. Experimental retention times were determined after reversed phase separation and peptide MS(2) data was acquired using a high-resolution mass spectrometer operated in data-dependent acquisition mode (DDA). A support vector regression model was trained using a combination of existing sequence-independent peptide descriptors and a newly derived set of selected amino acid index derived sequence-specific peptide (ASP) descriptors. The model was trained and validated using the experimental retention times of the 713 small food-relevant peptides prepared. Whilst selecting the most useful ASP descriptors for our model, special attention was given to predict the retention time differences between homologous peptide structures. Inclusion of ASP descriptors greatly improved the ability to accurately predict retention times, including retention time differences between 157 homologous peptide pairs. The final prediction model had a goodness-of-fit (Q(2)) of 0.94; moreover for 93% of the short peptides, the elution order was correctly predicted. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04670-2. Springer Berlin Heidelberg 2023-03-31 2023 /pmc/articles/PMC10185643/ /pubmed/37000211 http://dx.doi.org/10.1007/s00216-023-04670-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Paper
Hollebrands, Boudewijn
Hageman, Jos A.
van de Sande, Jasper W.
Albada, Bauke
Janssen, Hans-Gerd
Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title_full Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title_fullStr Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title_full_unstemmed Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title_short Improved LC–MS identification of short homologous peptides using sequence-specific retention time predictors
title_sort improved lc–ms identification of short homologous peptides using sequence-specific retention time predictors
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185643/
https://www.ncbi.nlm.nih.gov/pubmed/37000211
http://dx.doi.org/10.1007/s00216-023-04670-2
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