scholarly journals DIALib: an automated ion library generator for data independent acquisition mass spectrometry analysis of peptides and glycopeptides

2019 ◽  
Author(s):  
Toan K. Phung ◽  
Lucia F Zacchi ◽  
Benjamin L. Schulz

AbstractData Independent Acquisition (DIA) Mass Spectrometry (MS) workflows allow unbiased measurement of all detectable peptides from complex proteomes, but require ion libraries for interrogation of peptides of interest. These DIA ion libraries can be theoretical or built from peptide identification data from Data Dependent Acquisition (DDA) MS workflows. However, DDA libraries derived from empirical data rely on confident peptide identification, which can be challenging for peptides carrying complex post-translational modifications. Here, we present DIALib, software to automate the construction of peptide and glycopeptide Data Independent Acquisition ion Libraries. We show that DIALib theoretical ion libraries can identify and measure diverse N- and O-glycopeptides from yeast and mammalian glycoproteins without prior knowledge of the glycan structures present. We present proof-of-principle data from a moderately complex yeast cell wall glycoproteome and a simple mixture of mammalian glycoproteins. We also show that DIALib libraries consisting only of glycan oxonium ions can quickly and easily provide a global compositional glycosylation profile of the detectable “oxoniome” of glycoproteomes. DIALib will help enable DIA glycoproteomics as a complementary analytical approach to DDA glycoproteomics.

2009 ◽  
Vol 9 (1) ◽  
pp. 98 ◽  
Author(s):  
Tao Wu ◽  
Tiezheng Yuan ◽  
Sau-Na Tsai ◽  
Chunmei Wang ◽  
Sai-Ming Sun ◽  
...  

PROTEOMICS ◽  
2004 ◽  
Vol 4 (4) ◽  
pp. 961-969 ◽  
Author(s):  
Jane Razumovskaya ◽  
Victor Olman ◽  
Dong Xu ◽  
Edward C. Uberbacher ◽  
Nathan C. VerBerkmoes ◽  
...  

2016 ◽  
Vol 283 (1832) ◽  
pp. 20160593 ◽  
Author(s):  
Timothy P. Cleland ◽  
Elena R. Schroeter ◽  
Robert S. Feranec ◽  
Deepak Vashishth

Vertebrate fossils have been collected for hundreds of years and are stored in museum collections around the world. These remains provide a readily available resource to search for preserved proteins; however, the vast majority of palaeoproteomic studies have focused on relatively recently collected bones with a well-known handling history. Here, we characterize proteins from the nasal turbinates of the first Castoroides ohioensis skull ever discovered. Collected in 1845, this is the oldest museum-curated specimen characterized using palaeoproteomic tools. Our mass spectrometry analysis detected many collagen I peptides, a peptide from haemoglobin beta, and in vivo and diagenetic post-translational modifications. Additionally, the identified collagen I sequences provide enough resolution to place C. ohioensis within Rodentia. This study illustrates the utility of archived museum specimens for both the recovery of preserved proteins and phylogenetic analyses.


2015 ◽  
Vol 10 (Suppl 1) ◽  
pp. P53
Author(s):  
Marta Vilà-Rico ◽  
Sebastián Contesse ◽  
José E Barcena Llona ◽  
Ricardo Rojas-García ◽  
Fernando Valle ◽  
...  

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