A mass spectrometric method for in-depth profiling of phosphoinositide regioisomers and their disease-associated regulation.
Shin MoriokaHiroki NakanishiToshiyoshi YamamotoJunya HasegawaEmi TokudaTomoya HikitaTomoko SakiharaYuuki KugiiChitose OneyamaMasakazu YamazakiAkira SuzukiJunko SasakiTakehiko SasakiPublished in: Nature communications (2022)
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.
Keyphrases
- mass spectrometry
- fatty acid
- prostate cancer
- liquid chromatography
- single cell
- capillary electrophoresis
- high performance liquid chromatography
- poor prognosis
- multiple sclerosis
- high resolution
- cell proliferation
- gas chromatography
- early onset
- tandem mass spectrometry
- transcription factor
- reactive oxygen species
- ms ms
- high speed
- protein kinase
- pi k akt
- binding protein
- simultaneous determination
- long non coding rna