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A new SWATH ion library for mouse adult hippocampal neural stem cells
Over the last years, the SWATH data-independent acquisition protocol (Sequential Window acquisition of All THeoretical mass spectra) has become a cornerstone for the worldwide proteomics community (Collins et al., 2017) [1]. In this approach, a high-resolution quadrupole-ToF mass spectrometer acquir...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995750/ https://www.ncbi.nlm.nih.gov/pubmed/29896482 http://dx.doi.org/10.1016/j.dib.2018.02.062 |
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author | Braccia, Clarissa Espinal, Meritxell Pons Pini, Mattia De Pietri Tonelli, Davide Armirotti, Andrea |
author_facet | Braccia, Clarissa Espinal, Meritxell Pons Pini, Mattia De Pietri Tonelli, Davide Armirotti, Andrea |
author_sort | Braccia, Clarissa |
collection | PubMed |
description | Over the last years, the SWATH data-independent acquisition protocol (Sequential Window acquisition of All THeoretical mass spectra) has become a cornerstone for the worldwide proteomics community (Collins et al., 2017) [1]. In this approach, a high-resolution quadrupole-ToF mass spectrometer acquires thousands of MS/MS data by selecting not just a single precursor at a time, but by allowing a broad m/z range to be fragmented. This acquisition window is then sequentially moved from the lowest to the highest mass selection range. This technique enables the acquisition of thousands of high-resolution MS/MS spectra per minute in a standard LC–MS run. In the subsequent data analysis phase, the corresponding dataset is searched in a “triple quadrupole-like” mode, thus not considering the whole MS/MS scan spectrum, but by searching for several precursor to fragment transitions that identify and quantify the corresponding peptide. This search is made possible with the use of an ion library, previously acquired in a classical data dependent, full-spectrum mode (Fabre et al., 2017; Wu et al., 2017) [2], [3]. The SWATH protocol, combining the protein identification power of high-resolution MS/MS spectra with the robustness and accuracy in analyte quantification of triple-quad targeted workflows, has become very popular in proteomics research. The major drawback lies in the ion library itself, which is normally demanding and time-consuming to build. Conversely, through the realignment of chromatographic retention times, an ion library of a given proteome can relatively easily be tailored upon “any” proteomics experiment done on the same proteome. We are thus hereby sharing with the worldwide proteomics community our newly acquired ion library of mouse adult hippocampal neural stem cells. Given the growing effort in neuroscience research involving proteomics experiments (Pons-Espinal et al., 2017; Sarnyai and Guest, 2017; Sethi et al., 2015; Bramini et al., 2016) [4,[5], [6], [7], we believe that this data might be of great help for the neuroscience community. All the here reported data (RAW files, results and ion library) can be freely downloaded from the SWATHATLAS (Deutsch et al., 2008) [8] website (http://www.peptideatlas.org/PASS/PASS01110) |
format | Online Article Text |
id | pubmed-5995750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-59957502018-06-12 A new SWATH ion library for mouse adult hippocampal neural stem cells Braccia, Clarissa Espinal, Meritxell Pons Pini, Mattia De Pietri Tonelli, Davide Armirotti, Andrea Data Brief Proteomics and Biochemistry Over the last years, the SWATH data-independent acquisition protocol (Sequential Window acquisition of All THeoretical mass spectra) has become a cornerstone for the worldwide proteomics community (Collins et al., 2017) [1]. In this approach, a high-resolution quadrupole-ToF mass spectrometer acquires thousands of MS/MS data by selecting not just a single precursor at a time, but by allowing a broad m/z range to be fragmented. This acquisition window is then sequentially moved from the lowest to the highest mass selection range. This technique enables the acquisition of thousands of high-resolution MS/MS spectra per minute in a standard LC–MS run. In the subsequent data analysis phase, the corresponding dataset is searched in a “triple quadrupole-like” mode, thus not considering the whole MS/MS scan spectrum, but by searching for several precursor to fragment transitions that identify and quantify the corresponding peptide. This search is made possible with the use of an ion library, previously acquired in a classical data dependent, full-spectrum mode (Fabre et al., 2017; Wu et al., 2017) [2], [3]. The SWATH protocol, combining the protein identification power of high-resolution MS/MS spectra with the robustness and accuracy in analyte quantification of triple-quad targeted workflows, has become very popular in proteomics research. The major drawback lies in the ion library itself, which is normally demanding and time-consuming to build. Conversely, through the realignment of chromatographic retention times, an ion library of a given proteome can relatively easily be tailored upon “any” proteomics experiment done on the same proteome. We are thus hereby sharing with the worldwide proteomics community our newly acquired ion library of mouse adult hippocampal neural stem cells. Given the growing effort in neuroscience research involving proteomics experiments (Pons-Espinal et al., 2017; Sarnyai and Guest, 2017; Sethi et al., 2015; Bramini et al., 2016) [4,[5], [6], [7], we believe that this data might be of great help for the neuroscience community. All the here reported data (RAW files, results and ion library) can be freely downloaded from the SWATHATLAS (Deutsch et al., 2008) [8] website (http://www.peptideatlas.org/PASS/PASS01110) Elsevier 2018-02-27 /pmc/articles/PMC5995750/ /pubmed/29896482 http://dx.doi.org/10.1016/j.dib.2018.02.062 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Proteomics and Biochemistry Braccia, Clarissa Espinal, Meritxell Pons Pini, Mattia De Pietri Tonelli, Davide Armirotti, Andrea A new SWATH ion library for mouse adult hippocampal neural stem cells |
title | A new SWATH ion library for mouse adult hippocampal neural stem cells |
title_full | A new SWATH ion library for mouse adult hippocampal neural stem cells |
title_fullStr | A new SWATH ion library for mouse adult hippocampal neural stem cells |
title_full_unstemmed | A new SWATH ion library for mouse adult hippocampal neural stem cells |
title_short | A new SWATH ion library for mouse adult hippocampal neural stem cells |
title_sort | new swath ion library for mouse adult hippocampal neural stem cells |
topic | Proteomics and Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995750/ https://www.ncbi.nlm.nih.gov/pubmed/29896482 http://dx.doi.org/10.1016/j.dib.2018.02.062 |
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