We describe an algorithm which modifies a protein database such that during a database search deamidation is limited to asparagines strictly contained within the N-glycosylation consensus sequence. The modified database was evaluated using a dataset created from the shotgun proteomic analysis of N-linked glycopeptides from human blood serum. We demonstrate that the application of the modified database eliminates incorrect glycopeptide assignments, reduces the peptide false-discovery rate, and eliminates the need for manual validation of glycopeptide identifications. Copyright © 2005 John Wiley & Sons, Ltd
Thesis (Ph.D.)--University of Washington, 2022Over the last 30 years, the field of computational mas...
Protein glycosylation accounts for one of the most complex protein modifications, of which aberrant ...
Study of site-specific N-glycosylation in complex sample remains a huge analytical challenge because...
We describe an algorithm which modifies a protein database such that during a database search deamid...
Workflows capable of determining glycopeptides in large-scale are missing in the field of glycoprote...
In the field of glycoproteomic glycosylation and glycopeptides are essential for people to study. It...
ABSTRACT: Glycoproteins are biologically significant large molecules that participate in numerous ce...
Advances in software-driven glycopeptide identification have facilitated N-glycoproteomics studies r...
Confident characterization of intact glycopeptides is a challenging task in mass spectrometry-based ...
The detailed characterization of site-specific glycosylation requires the identification of glycan c...
Glycosylation is a common protein modification with a significant role in many vital cellular proces...
The leading proteomic method for identifying N-glycosylated peptides is liquid chromatography couple...
Glycosylation is an important protein modification that involves enzymatic attachment of sugars to a...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The emergence of tandem mass spectrometry (MS/MS) technology has significantly accelerated protein i...
Thesis (Ph.D.)--University of Washington, 2022Over the last 30 years, the field of computational mas...
Protein glycosylation accounts for one of the most complex protein modifications, of which aberrant ...
Study of site-specific N-glycosylation in complex sample remains a huge analytical challenge because...
We describe an algorithm which modifies a protein database such that during a database search deamid...
Workflows capable of determining glycopeptides in large-scale are missing in the field of glycoprote...
In the field of glycoproteomic glycosylation and glycopeptides are essential for people to study. It...
ABSTRACT: Glycoproteins are biologically significant large molecules that participate in numerous ce...
Advances in software-driven glycopeptide identification have facilitated N-glycoproteomics studies r...
Confident characterization of intact glycopeptides is a challenging task in mass spectrometry-based ...
The detailed characterization of site-specific glycosylation requires the identification of glycan c...
Glycosylation is a common protein modification with a significant role in many vital cellular proces...
The leading proteomic method for identifying N-glycosylated peptides is liquid chromatography couple...
Glycosylation is an important protein modification that involves enzymatic attachment of sugars to a...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
The emergence of tandem mass spectrometry (MS/MS) technology has significantly accelerated protein i...
Thesis (Ph.D.)--University of Washington, 2022Over the last 30 years, the field of computational mas...
Protein glycosylation accounts for one of the most complex protein modifications, of which aberrant ...
Study of site-specific N-glycosylation in complex sample remains a huge analytical challenge because...