Unlocking the Neuropeptidome using a Novel Endogenous Peptidomics Framework
Fields, L.; Wu, W.; Dang, T. C.; Ibarra, A. E.; Gray, M.; Li, L.
Show abstract
Endogenous peptides have garnered increasing attention over the past decade driven by the development of advanced analytical methods. However, large-scale investigations of peptides as potential disease biomarkers or drug candidates are still hindered by their challenging biochemical properties and the scarcity of specialized analytical tools. Among these, neuropeptides are particularly challenging to study due to their low in vivo concentration, rapid turnover rate, and high structural variability. Data-independent acquisition (DIA) mass spectrometry (MS) has shown great ability in profiling low-abundance ions. Nevertheless, most available DIA analytical tools are designed for proteomics studies and are not suitable for endogenous peptides, as there is no set enzymatic cleavage for these peptides. Here, we introduce the novel EndoGenius platform, paired with DIA-NN, to achieve high-confidence neuropeptide identification using an updated spectral library for DIA MS analysis. By employing orthogonal offline fractionation, ion mobility instrumentation, and an optimized database searching algorithm specifically for neuropeptides, we have constructed the largest crustacean neuropeptide spectral library to date. With this library, in combination with neural networking technology, we report a 100-fold increase in the number of neuropeptides identified in all Cancer borealis tissues analyzed. We also cross-validated these findings with transcriptomics data to enhance identification confidence. This workflow presents a novel analytical framework for DIA peptidomics analysis, offering a robust approach to studying neuropeptides and other endogenous peptides. TOC O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=140 SRC="FIGDIR/small/659356v1_ufig1.gif" ALT="Figure 1"> View larger version (28K): org.highwire.dtl.DTLVardef@1bae342org.highwire.dtl.DTLVardef@9e26d8org.highwire.dtl.DTLVardef@1084f06org.highwire.dtl.DTLVardef@7c1371_HPS_FORMAT_FIGEXP M_FIG C_FIG SynopsisWe present a framework that capitalizes on robust analytical innovations and an optimized bioinformatics pipeline to provide the most comprehensive snapshot of the crustacean neuropeptidome to-date.
Matching journals
The top 1 journal accounts for 50% of the predicted probability mass.
Similar papers in this journal
- A comprehensive LFQ benchmark dataset on modern day acquisition strategies in proteomics 98%
- Implementing the re-use of public DIA proteomics datasets: from the PRIDE database to Expression Atlas 96%
- An interactive mass spectrometry atlas of histone posttranslational modifications in T-cell acute leukemia 96%
Similar papers in this journal
- Automating data analysis for hydrogen/deuterium exchange mass spectrometry using data-independent acquisition methodology 96%
- Single Cell Proteomics Using a Trapped Ion Mobility Time-of-Flight Mass Spectrometer Provides Insight into the Post-translational Modification Landscape of Individual Human Cells 96%
- OzFAD: Ozone-enabled fatty acid discovery reveals unexpected diversity in the human lipidome 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.