Data-Independent Acquisition (DIA) Is Superior for High Precision Phospho-Peptide Quantification in Magnaporthe oryzae

• Published in: Journal of fungi (Basel) Vol. 9; no. 1; p. 63
• Main Authors: Bersching, Katharina, Michna, Thomas, Tenzer, Stefan, Jacob, Stefan
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 31.12.2022; MDPI
• Subjects: Accuracy; Algorithms; Amino acids; Bioinformatics; cellular signaling; Chromatography; Communication; Data processing; LC-MS/MS; Magnaporthe oryzae; Mass spectrometry; Peptides; phospho-peptide enrichment; Phosphorylation; Proteins; Proteomics; Scientific imaging; Signal transduction; Software; United States > US; DDA; LC-MS/MS; phospho-peptide enrichment; phospho-peptidomics; proteomics; bioinformatics; Magnaporthe oryzae; cellular signaling; DIA; phosphorylation
• ISSN: 2309-608X; 2309-608X
• DOI: 10.3390/jof9010063

The dynamic interplay of signaling networks in most major cellular processes is characterized by the orchestration of reversible protein phosphorylation. Consequently, analytic methods such as quantitative phospho-peptidomics have been pushed forward from a highly specialized edge-technique to a powerful and versatile platform for comprehensively analyzing the phosphorylation profile of living organisms. Despite enormous progress in instrumentation and bioinformatics, a high number of missing values caused by the experimental procedure remains a major problem, due to either a random phospho-peptide enrichment selectivity or borderline signal intensities, which both cause the exclusion for fragmentation using the commonly applied data dependent acquisition (DDA) mode. Consequently, an incomplete dataset reduces confidence in the subsequent statistical bioinformatic processing. Here, we successfully applied data independent acquisition (DIA) by using the filamentous fungus as a model organism, and could prove that while maintaining data quality (such as phosphosite and peptide sequence confidence), the data completeness increases dramatically. Since the method presented here reduces the LC-MS/MS analysis from 3 h to 1 h and increases the number of phosphosites identified up to 10-fold in contrast to published studies in , we provide a refined methodology and a sophisticated resource for investigation of signaling processes in filamentous fungi.