4.7 Article

Direct introduction MALDI FTICR MS based on dried droplet deposition applied to non-targeted metabolomics on Pisum Sativum root exudates

Journal

TALANTA
Volume 253, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2022.123901

Keywords

Root exudates; Non-targeted metabolomics; MALDI; Pisum sativum; Fourier transform ion cyclotron resonance mass spectrometry

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In this study, the performance of direct introduction electrospray ionization (ESI) and matrix assisted laser desorption ionization (MALDI) coupled with Fourier-Transform ion cyclotron resonance mass spectrometry (FTICR MS) for analyzing root exudates (RE) was systematically evaluated. MALDI showed better salt tolerance and ionization efficiency at high salinity, making it suitable for analyzing metabolites in complex matrices. The study also demonstrated the complementarity of the two ionization sources and the advantage of MALDI in detecting metabolites suffering from matrix effects in ESI mode.
Non-targeted metabolomic approaches based on direct introduction (DI) through a soft ionization source are nowadays used for large-scale analysis and wide cover-up of metabolites in complex matrices. When coupled with ultra-high-resolution Fourier-Transform ion cyclotron resonance (FTICR MS), DI is generally performed through electrospray (ESI), which, despite the great analytical throughput, can suffer of matrix effects due to residual salts or charge competitors. In alternative, matrix assisted laser desorption ionization (MALDI) coupled with FTICR MS offers relatively high salt tolerance but it is mainly used for imaging of small molecule within biological tissues. In this study, we report a systematic evaluation on the performance of direct introduction ESI and MALDI coupled with FTICR MS applied to the analysis of root exudates (RE), a complex mixture of me-tabolites released from plant root tips and containing a relatively high salt concentration. Classic dried droplet deposition followed by screening of best matrices and ratio allowed the selection of high ranked conditions for non-targeted metabolomics on RE. Optimization of MALDI parameters led to improved reproducibility and precision. A RE desalted sample was used for comparison on ionization efficiency of the two sources and ion enhancement at high salinity was highlighted in MALDI by spiking desalted solution with inorganic salts. Application of a true lyophilized RE sample exhibited the complementarity of the two sources and the ability of MALDI in the detection of undisclosed metabolites suffering of matrix effects in ESI mode.

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