Triple acquisition mass spectrometry (TRAM) combining targeted and non-targeted metabolomics in a single run
We introduce TRAM, a triple acquisition strategy on a high-speed quadrupole time-of-flight mass spectrometer for merging non-targeted and targeted metabolomics into one run. TRAM stands for “quasi-simultaneous” acquisition of (1) a full scan MS1, (2) top 30 data-dependent MS2 (DDA), and (3) targeted...
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Veröffentlicht in: | Analytica chimica acta 2024-12, Vol.1331, p.343314, Article 343314 |
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Zusammenfassung: | We introduce TRAM, a triple acquisition strategy on a high-speed quadrupole time-of-flight mass spectrometer for merging non-targeted and targeted metabolomics into one run. TRAM stands for “quasi-simultaneous” acquisition of (1) a full scan MS1, (2) top 30 data-dependent MS2 (DDA), and (3) targeted scheduled MS2 for multiple reaction monitoring (MRM) within measurement cycles of ∼1 s. TRAM combines the selectivity and sensitivity of state-of-the-art targeted MRM-based methods with the full scope of non-targeted analysis enabled by high-resolution mass spectrometry.
In this work, we deploy a workflow based on hydrophilic interaction liquid chromatography (HILIC). For a broad panel of metabolites, we provide chromatographic retention times, and optimized conditions as a basis for targeted MRM experiments, listing accurate masses and sum formulas for fragment ions (including fully 13C labeled analogs). Validation experiments showed that TRAM offered (1) linear working ranges and limits of quantification comparable to MRM-only methods, (2) enabled accurate quantification in SRM 1950 human plasma reference material, and (3) was equivalent to DDA-only approaches in non-targeted metabolomics. Metabolomics in human cerebrospinal fluid showcased the power of the strategy, emphasizing the need for high coverage/high throughput metabolomics in clinical studies.
Acquiring up to 30 data-dependent spectra per MS cycle while still offering gold standard absolute quantification down to low nanomolar concentrations, TRAM allows in-depth profiling and reduces required sample volume, time, cost, and environmental impact.
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•High-speed triple acquisition strategy unifies targeted & non-targeted metabolomics.•Absolute quantification & high number of DDA MS2 scans for individual samples.•TRAM unites MS1, DDA-MS2 & MRM-MS2 data acquisition within a single injection.•TRAM was benchmarked using SRM 1950 & cerebrospinal fluid of meningioma patients.•Optimized MRM parameters & HILIC – retention times for more than 90 metabolites. |
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ISSN: | 0003-2670 1873-4324 1873-4324 |
DOI: | 10.1016/j.aca.2024.343314 |