Quantitative Targeted Metabolomics for 15d-deoxy-Δ12, 14-PGJ2 (15dPGJ2) by MALDI-MS
2017
Kim, K.J., Soongsil University, Seoul, Republic of Korea | Park, H.G., Soongsil University, Seoul, Republic of Korea | Hwang, C.H., Soongsil University, Seoul, Republic of Korea | Ann, D.H., Soongsil University, Seoul, Republic of Korea | Song, W.S., Seoul National University, Seoul, Republic of Korea | Choi, K.Y., Ajou University, Seoul, Republic of Korea | Yang, Y.H., Ajou University, Seoul, Republic of Korea | Park, S.Y., Soongsil University, Seoul, Republic of Korea | Kim, Y.G., Soongsil University, Seoul, Republic of Korea
Prostaglandins (PGs) are lipid mediators that may play important roles in cancer, immunomodulation, and neurodegeneration. So, the quantitative analysis of PGs will therefore be important in order to understand the natural history of a range of diseases and may be used as a tool in the development of new biotherapeutics. However, such an analysis is problematic because of the small quantities of PGs present in the body. Here, we developed a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-MS)-based analytical method for rapid and easy quantification of the ketone-containing PGs (15d-PGJ₂ etc.) as a targeted metabolomics platform. The chemical derivatization with Girard's reagent P (GP) provided a good linearity (R² greater than 0.99) between peak area and quantity of 15d-PGJ₂ and highly improved sensitivity (limit of quantitation, LOQ: 1.25 pmol on a spot in MALDI plate). Finally, we utilized this method to directly characterize the interaction between peroxisome proliferatoractivated receptor gamma-ligand binding domain (PPARγLBD) and 15d-PGJ₂. The 15d-PGJ₂ was enriched by PPARgamma-LBD and also the binding level of the ligand was dropped considerably by the treatment of PPARγ agonist such as rosiglitazone (about 0.61-fold reduction). Taken together, our MALDI-MS-based targeted metabolomics method for ketone-containing PGs may be applicable to elucidate the protein-metabolite interactions and to identify natural ligands for drug candidates.
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