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Teschner, D.

Publications and source records attributed to Teschner, D..

3 recordsLinked to original sources

Cross-Domain Transfer Learning from Peptides to Lipids Using a Multi-Property Fine-Tuned LLM

Accurate knowledge of liquid chromatography retention time (RT) is essential for confident compound identification in metabolomics and lipidomics. Yet, it is often constrained by the scarcity of experimental data for many molecular classes. Current workflows depend on experimental RT libraries, which are time-consuming to build and limited to previously observed compounds. Here, we present a transfer learning pipeline that leverages large, publicly available peptide datasets to enable accurate lipid RT prediction in data-sparse scenarios. We first show that a ChemBERTa language model, when pre-trained on peptides with a multi-task objective (predicting both RT and fundamental RDKit molecular descriptors), learns a more robust and generalizable chemical representation than a single-task (RT-only) model. This multi-property pre-training yielded superior generalization in lipids, achieving test R2 values of 0.842 against 0.814 (RT-only). Crucially, transferring this peptide-based model to lipid data provided a pronounced advantage in data-sparse scenarios. When fine-tuned on only 5% of available lipid data, the transferred model improved the median test R2 by +0.234 over a model trained from scratch. Significant benefits persisted at intermediate data scales (50-75%), with performance converging only when 100% of the lipid data was used. Notably, the pre-trained model never underperformed the baseline, exhibiting more stable training across all data scales. These results demonstrate that multi-property pre-training guides language models towards chemically meaningful representations that support better RT prediction in different molecular domains. Furthermore, peptide-based pre-training facilitates cross-domain transfer of chemical properties to lipid. Our work provides a practical, scalable strategy to mitigate data scarcity in lipidomics by transferring knowledge from data-rich peptide databases, offering a computational alternative to extensive experimental library generation and enabling more confident identification in small-scale omics studies.

bioinformatics↗

midiaPASEF maximizes information content in data-independent acquisition proteomics

Data-independent acquisition (DIA) approaches provide comprehensive records of all detectable pre-cursor and fragment ions. Here we introduce midiaPASEF, a novel DIA scan mode using mobility-specific micro-encoding of overlapping quadrupole windows to optimally cover the ion population in the ion mobility-mass to charge plane. Using overlapping ion mobility-encoded quadrupole windows, midiaPASEF maximizes information content in DIA acquisitions which enables the determination of the precursor m/z of each fragment ion with a precision of less than 2 Th. The Snakemake-based MIDIAID pipeline integrates algorithms for multidimensional peak detection and for machine-learning-based classification of precursor-fragment relationships. The MIDIAID pipeline enables fully automated processing and multidimensional deconvolution of midia-PASEF files and exports highly specific DDA-like MSMS spectra which are suitable for de novo sequencing and can be searched directly with established tools including PEAKS, FragPipe and Mascot. midiaPASEF acquisition identifies over 40 unique peptides per second and provides powerful library-free DIA analyses including phosphopeptidome and immunopeptidome samples.

bioinformatics↗

Locality-sensitive hashing enables signal classification in high-throughput mass spectrometry raw data at scale

Mass spectrometry is an important experimental technique in the field of proteomics. However, analysis of certain mass spectrometry data faces a combination of two challenges: First, even a single experiment produces a large amount of multi-dimensional raw data and, second, signals of interest are not single peaks but patterns of peaks that span along the different dimensions. The rapidly growing amount of mass spectrometry data increases the demand for scalable solutions. Existing approaches for signal detection are usually not well suited for processing large amounts of data in parallel or rely on strong assumptions concerning the signals properties. In this study, it is shown that locality-sensitive hashing enables signal classification in mass spectrometry raw data at scale. Through appropriate choice of algorithm parameters it is possible to balance false-positive and false-negative rates. On synthetic data, a superior performance compared to an intensity thresholding approach was achieved. The implementation scaled out up to 88 threads on real data. Locality-sensitive hashing is a desirable approach for signal classification in mass spectrometry raw data. Generated data and code are available at https://github.com/hildebrandtlab/mzBucket. Raw data is available at https://zenodo.org/record/5036526.

bioinformatics↗