{"title":"Software Design and Analytical Challenges for Confident Glycopeptide Identification With Data-Independent Acquisition.","authors":"Mary Rachel Nalehua, Joseph Zaia","doi":"10.1002/mas.70000","DOIUrl":null,"url":null,"abstract":"<p><p>Glycosylation is an abundant post-translational modification that impacts a wide variety of functions, including protein regulation, cell adhesion, and structural integrity. The application of proteomics methods to glycopeptide assignment faces unique challenges due to high heterogeneity, which results in complex populations with low overall abundance per glycopeptide. In addition, glycans dissociate at a lower collision energy compared to their attached peptide component. The resulting mass spectral data require specialized assignment software, which has caused glycoproteomics to lag traditional proteomics. Existing software primarily focuses on data-dependent acquisition (DDA), but manual validation is frequently required, and experiments are necessarily limited by the stochastic nature of DDA ion-selection. Data-independent acquisition (DIA) allows for a more complete and robust analysis of glycopeptide samples, but analysis software is still sparse. In this review, we discuss the current state of DDA analysis software, the limitations, and how it can inform our forays into DIA glycoproteomics.</p>","PeriodicalId":206,"journal":{"name":"Mass Spectrometry Reviews","volume":" ","pages":""},"PeriodicalIF":6.6000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mass Spectrometry Reviews","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/mas.70000","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
引用次数: 0
Abstract
Glycosylation is an abundant post-translational modification that impacts a wide variety of functions, including protein regulation, cell adhesion, and structural integrity. The application of proteomics methods to glycopeptide assignment faces unique challenges due to high heterogeneity, which results in complex populations with low overall abundance per glycopeptide. In addition, glycans dissociate at a lower collision energy compared to their attached peptide component. The resulting mass spectral data require specialized assignment software, which has caused glycoproteomics to lag traditional proteomics. Existing software primarily focuses on data-dependent acquisition (DDA), but manual validation is frequently required, and experiments are necessarily limited by the stochastic nature of DDA ion-selection. Data-independent acquisition (DIA) allows for a more complete and robust analysis of glycopeptide samples, but analysis software is still sparse. In this review, we discuss the current state of DDA analysis software, the limitations, and how it can inform our forays into DIA glycoproteomics.
期刊介绍:
The aim of the journal Mass Spectrometry Reviews is to publish well-written reviews in selected topics in the various sub-fields of mass spectrometry as a means to summarize the research that has been performed in that area, to focus attention of other researchers, to critically review the published material, and to stimulate further research in that area.
The scope of the published reviews include, but are not limited to topics, such as theoretical treatments, instrumental design, ionization methods, analyzers, detectors, application to the qualitative and quantitative analysis of various compounds or elements, basic ion chemistry and structure studies, ion energetic studies, and studies on biomolecules, polymers, etc.