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AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation

[Image: see text] Protein quantitation via mass spectrometry relies on peptide proxies for the parent protein from which abundances are estimated. Owing to the variability in signal from individual peptides, accurate absolute quantitation usually relies on the addition of an external standard. Typic...

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Autores principales: Rusilowicz, Martin, Newman, David W., Creamer, Declan R., Johnson, James, Adair, Kareena, Harman, Victoria M., Grant, Chris M., Beynon, Robert J., Hubbard, Simon J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903321/
https://www.ncbi.nlm.nih.gov/pubmed/36688735
http://dx.doi.org/10.1021/acs.jproteome.2c00608
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author Rusilowicz, Martin
Newman, David W.
Creamer, Declan R.
Johnson, James
Adair, Kareena
Harman, Victoria M.
Grant, Chris M.
Beynon, Robert J.
Hubbard, Simon J.
author_facet Rusilowicz, Martin
Newman, David W.
Creamer, Declan R.
Johnson, James
Adair, Kareena
Harman, Victoria M.
Grant, Chris M.
Beynon, Robert J.
Hubbard, Simon J.
author_sort Rusilowicz, Martin
collection PubMed
description [Image: see text] Protein quantitation via mass spectrometry relies on peptide proxies for the parent protein from which abundances are estimated. Owing to the variability in signal from individual peptides, accurate absolute quantitation usually relies on the addition of an external standard. Typically, this involves stable isotope-labeled peptides, delivered singly or as a concatenated recombinant protein. Consequently, the selection of the most appropriate surrogate peptides and the attendant design in recombinant proteins termed QconCATs are challenges for proteome science. QconCATs can now be built in a “a-la-carte” assembly method using synthetic biology: ALACATs. To assist their design, we present “AlacatDesigner”, a tool that supports the peptide selection for recombinant protein standards based on the user’s target protein. The user-customizable tool considers existing databases, occurrence in the literature, potential post-translational modifications, predicted miscleavage, predicted divergence of the peptide and protein quantifications, and ionization potential within the mass spectrometer. We show that peptide selections are enriched for good proteotypic and quantotypic candidates compared to empirical data. The software is freely available to use either via a web interface AlacatDesigner, downloaded as a Desktop application or imported as a Python package for the command line interface or in scripts.
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spelling pubmed-99033212023-02-08 AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation Rusilowicz, Martin Newman, David W. Creamer, Declan R. Johnson, James Adair, Kareena Harman, Victoria M. Grant, Chris M. Beynon, Robert J. Hubbard, Simon J. J Proteome Res [Image: see text] Protein quantitation via mass spectrometry relies on peptide proxies for the parent protein from which abundances are estimated. Owing to the variability in signal from individual peptides, accurate absolute quantitation usually relies on the addition of an external standard. Typically, this involves stable isotope-labeled peptides, delivered singly or as a concatenated recombinant protein. Consequently, the selection of the most appropriate surrogate peptides and the attendant design in recombinant proteins termed QconCATs are challenges for proteome science. QconCATs can now be built in a “a-la-carte” assembly method using synthetic biology: ALACATs. To assist their design, we present “AlacatDesigner”, a tool that supports the peptide selection for recombinant protein standards based on the user’s target protein. The user-customizable tool considers existing databases, occurrence in the literature, potential post-translational modifications, predicted miscleavage, predicted divergence of the peptide and protein quantifications, and ionization potential within the mass spectrometer. We show that peptide selections are enriched for good proteotypic and quantotypic candidates compared to empirical data. The software is freely available to use either via a web interface AlacatDesigner, downloaded as a Desktop application or imported as a Python package for the command line interface or in scripts. American Chemical Society 2023-01-23 /pmc/articles/PMC9903321/ /pubmed/36688735 http://dx.doi.org/10.1021/acs.jproteome.2c00608 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Rusilowicz, Martin
Newman, David W.
Creamer, Declan R.
Johnson, James
Adair, Kareena
Harman, Victoria M.
Grant, Chris M.
Beynon, Robert J.
Hubbard, Simon J.
AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title_full AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title_fullStr AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title_full_unstemmed AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title_short AlacatDesigner—Computational Design of Peptide Concatamers for Protein Quantitation
title_sort alacatdesigner—computational design of peptide concatamers for protein quantitation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903321/
https://www.ncbi.nlm.nih.gov/pubmed/36688735
http://dx.doi.org/10.1021/acs.jproteome.2c00608
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