Phosphoinositides are minor components of cell membranes, but play crucial roles in numerous signal transduction pathways. To obtain quantitative measures of phosphoinositides, sensitive, accurate, and comprehensive methods are needed. Here, we present a quantitative targeted ion chromatography-mass spectrometry-based workflow that separates phosphoinositide isomers and increases the quantitative accuracy of measured phosphoinositides. Besides testing different analytical characteristics such as extraction and separation efficiency, the reproducibility of the developed workflow was also investigated. The workflow was verified in resting and stimulated human platelets, fat cells, and rat hippocampal brain tissue, where the LOD and LOQ for phosphoinositides were at 312.5 and 625 fmol, respectively. The robustness of the workflow is shown with different applications that confirms its suitability to analyze multiple less-abundant phosphoinositides.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280744PMC
http://dx.doi.org/10.1021/acs.jproteome.1c00017DOI Listing

Publication Analysis

Top Keywords

phosphoinositides
5
targeted phosphoinositides
4
phosphoinositides analysis
4
analysis high-performance
4
high-performance ion
4
ion chromatography-coupled
4
chromatography-coupled selected
4
selected reaction
4
reaction monitoring
4
monitoring mass
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!