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In-Depth Serum Proteomics by DIA-MS with In Silico Spectral Libraries Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic Arthritis
[Image: see text] In serum proteomics using mass spectrometry, the number of detectable proteins is reduced due to high-abundance proteins, such as albumin. However, recently developed data-independent acquisition mass spectrometry (DIA-MS) proteomics technology has made it possible to remarkably im...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892657/ https://www.ncbi.nlm.nih.gov/pubmed/35252692 http://dx.doi.org/10.1021/acsomega.1c06681 |
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author | Sato, Hironori Inoue, Yuzaburo Kawashima, Yusuke Nakajima, Daisuke Ishikawa, Masaki Konno, Ryo Nakamura, Ren Kato, Daigo Mitsunaga, Kanako Yamamoto, Takeshi Yamaide, Akiko Tomiita, Minako Hoshioka, Akira Ohara, Osamu Shimojo, Naoki |
author_facet | Sato, Hironori Inoue, Yuzaburo Kawashima, Yusuke Nakajima, Daisuke Ishikawa, Masaki Konno, Ryo Nakamura, Ren Kato, Daigo Mitsunaga, Kanako Yamamoto, Takeshi Yamaide, Akiko Tomiita, Minako Hoshioka, Akira Ohara, Osamu Shimojo, Naoki |
author_sort | Sato, Hironori |
collection | PubMed |
description | [Image: see text] In serum proteomics using mass spectrometry, the number of detectable proteins is reduced due to high-abundance proteins, such as albumin. However, recently developed data-independent acquisition mass spectrometry (DIA-MS) proteomics technology has made it possible to remarkably improve the number of proteins in a serum analysis by removing high-abundance proteins. Using this technology, we analyzed sera from patients with systemic juvenile idiopathic arthritis (sJIA), a rare pediatric disease. As a result, we identified 2727 proteins with a wide dynamic range derived from various tissue leakages. We also selected 591 proteins that differed significantly in their active phases. These proteins were involved in many inflammatory processes, and we also identified immunoproteasomes, which were not previously found in serum, suggesting that they may be involved in the pathogenesis of sJIA. A detailed high-depth DIA-MS proteomic analysis of serum may be useful for understanding the pathogenesis of sJIA and may provide clues for the development of new biomarkers. |
format | Online Article Text |
id | pubmed-8892657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88926572022-03-03 In-Depth Serum Proteomics by DIA-MS with In Silico Spectral Libraries Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic Arthritis Sato, Hironori Inoue, Yuzaburo Kawashima, Yusuke Nakajima, Daisuke Ishikawa, Masaki Konno, Ryo Nakamura, Ren Kato, Daigo Mitsunaga, Kanako Yamamoto, Takeshi Yamaide, Akiko Tomiita, Minako Hoshioka, Akira Ohara, Osamu Shimojo, Naoki ACS Omega [Image: see text] In serum proteomics using mass spectrometry, the number of detectable proteins is reduced due to high-abundance proteins, such as albumin. However, recently developed data-independent acquisition mass spectrometry (DIA-MS) proteomics technology has made it possible to remarkably improve the number of proteins in a serum analysis by removing high-abundance proteins. Using this technology, we analyzed sera from patients with systemic juvenile idiopathic arthritis (sJIA), a rare pediatric disease. As a result, we identified 2727 proteins with a wide dynamic range derived from various tissue leakages. We also selected 591 proteins that differed significantly in their active phases. These proteins were involved in many inflammatory processes, and we also identified immunoproteasomes, which were not previously found in serum, suggesting that they may be involved in the pathogenesis of sJIA. A detailed high-depth DIA-MS proteomic analysis of serum may be useful for understanding the pathogenesis of sJIA and may provide clues for the development of new biomarkers. American Chemical Society 2022-02-15 /pmc/articles/PMC8892657/ /pubmed/35252692 http://dx.doi.org/10.1021/acsomega.1c06681 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Sato, Hironori Inoue, Yuzaburo Kawashima, Yusuke Nakajima, Daisuke Ishikawa, Masaki Konno, Ryo Nakamura, Ren Kato, Daigo Mitsunaga, Kanako Yamamoto, Takeshi Yamaide, Akiko Tomiita, Minako Hoshioka, Akira Ohara, Osamu Shimojo, Naoki In-Depth Serum Proteomics by DIA-MS with In Silico Spectral Libraries Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic Arthritis |
title | In-Depth Serum Proteomics by DIA-MS with In
Silico Spectral Libraries
Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic
Arthritis |
title_full | In-Depth Serum Proteomics by DIA-MS with In
Silico Spectral Libraries
Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic
Arthritis |
title_fullStr | In-Depth Serum Proteomics by DIA-MS with In
Silico Spectral Libraries
Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic
Arthritis |
title_full_unstemmed | In-Depth Serum Proteomics by DIA-MS with In
Silico Spectral Libraries
Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic
Arthritis |
title_short | In-Depth Serum Proteomics by DIA-MS with In
Silico Spectral Libraries
Reveals Dynamics during the Active Phase of Systemic Juvenile Idiopathic
Arthritis |
title_sort | in-depth serum proteomics by dia-ms with in
silico spectral libraries
reveals dynamics during the active phase of systemic juvenile idiopathic
arthritis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892657/ https://www.ncbi.nlm.nih.gov/pubmed/35252692 http://dx.doi.org/10.1021/acsomega.1c06681 |
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