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A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation
Phosphoinositides are a family of membrane lipids essential for many biological and pathological processes. Due to the existence of multiple phosphoinositide regioisomers and their low intracellular concentrations, profiling these lipids and linking a specific acyl variant to a change in biological...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749000/ https://www.ncbi.nlm.nih.gov/pubmed/35013169 http://dx.doi.org/10.1038/s41467-021-27648-z |
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author | Morioka, Shin Nakanishi, Hiroki Yamamoto, Toshiyoshi Hasegawa, Junya Tokuda, Emi Hikita, Tomoya Sakihara, Tomoko Kugii, Yuuki Oneyama, Chitose Yamazaki, Masakazu Suzuki, Akira Sasaki, Junko Sasaki, Takehiko |
author_facet | Morioka, Shin Nakanishi, Hiroki Yamamoto, Toshiyoshi Hasegawa, Junya Tokuda, Emi Hikita, Tomoya Sakihara, Tomoko Kugii, Yuuki Oneyama, Chitose Yamazaki, Masakazu Suzuki, Akira Sasaki, Junko Sasaki, Takehiko |
author_sort | Morioka, Shin |
collection | PubMed |
description | Phosphoinositides are a family of membrane lipids essential for many biological and pathological processes. Due to the existence of multiple phosphoinositide regioisomers and their low intracellular concentrations, profiling these lipids and linking a specific acyl variant to a change in biological state have been difficult. To enable the comprehensive analysis of phosphoinositide phosphorylation status and acyl chain identity, we develop PRMC-MS (Phosphoinositide Regioisomer Measurement by Chiral column chromatography and Mass Spectrometry). Using this method, we reveal a severe skewing in acyl chains in phosphoinositides in Pten-deficient prostate cancer tissues, extracellular mobilization of phosphoinositides upon expression of oncogenic PIK3CA, and a unique profile for exosomal phosphoinositides. Thus, our approach allows characterizing the dynamics of phosphoinositide acyl variants in intracellular and extracellular milieus. |
format | Online Article Text |
id | pubmed-8749000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87490002022-01-20 A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation Morioka, Shin Nakanishi, Hiroki Yamamoto, Toshiyoshi Hasegawa, Junya Tokuda, Emi Hikita, Tomoya Sakihara, Tomoko Kugii, Yuuki Oneyama, Chitose Yamazaki, Masakazu Suzuki, Akira Sasaki, Junko Sasaki, Takehiko Nat Commun Article Phosphoinositides are a family of membrane lipids essential for many biological and pathological processes. Due to the existence of multiple phosphoinositide regioisomers and their low intracellular concentrations, profiling these lipids and linking a specific acyl variant to a change in biological state have been difficult. To enable the comprehensive analysis of phosphoinositide phosphorylation status and acyl chain identity, we develop PRMC-MS (Phosphoinositide Regioisomer Measurement by Chiral column chromatography and Mass Spectrometry). Using this method, we reveal a severe skewing in acyl chains in phosphoinositides in Pten-deficient prostate cancer tissues, extracellular mobilization of phosphoinositides upon expression of oncogenic PIK3CA, and a unique profile for exosomal phosphoinositides. Thus, our approach allows characterizing the dynamics of phosphoinositide acyl variants in intracellular and extracellular milieus. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8749000/ /pubmed/35013169 http://dx.doi.org/10.1038/s41467-021-27648-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Morioka, Shin Nakanishi, Hiroki Yamamoto, Toshiyoshi Hasegawa, Junya Tokuda, Emi Hikita, Tomoya Sakihara, Tomoko Kugii, Yuuki Oneyama, Chitose Yamazaki, Masakazu Suzuki, Akira Sasaki, Junko Sasaki, Takehiko A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title | A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title_full | A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title_fullStr | A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title_full_unstemmed | A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title_short | A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
title_sort | mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749000/ https://www.ncbi.nlm.nih.gov/pubmed/35013169 http://dx.doi.org/10.1038/s41467-021-27648-z |
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