Journal
NATURE COMMUNICATIONS
Volume 13, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41467-021-27648-z
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Funding
- JSPS [26670132, 15H04693, 20H04920, 26253006, 15H05899, 17H03980, 20H03433]
- AMED [18gm0710002h0006]
- Takeda Science Foundation
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A new method called PRMC-MS has been developed to analyze the dynamics of phosphoinositide acyl variants. The study reveals specific changes in acyl chains in prostate cancer tissues with PTEN deficiency and upon expression of oncogenic PIK3CA.
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.
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