Bottom up proteomics of cryptocyanin protein and anti-tumor Thomsen–Friedenreich neoglycoconjugate vaccine
In this thesis, two different kinds of complex biomolecules were examined: cryptocyanin protein of snow crab (Chionoecetes opilio) and carbohydrate-protein neoglycoconjugate vaccine using mass spectrometry (MS) and tandem mass spectrometry (MS/MS). The main objective of the first study was to determ...
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| Format: | Thesis |
| Language: | English |
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Memorial University of Newfoundland
2015
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| Online Access: | https://research.library.mun.ca/8396/ https://research.library.mun.ca/8396/1/thesis.pdf |
| Summary: | In this thesis, two different kinds of complex biomolecules were examined: cryptocyanin protein of snow crab (Chionoecetes opilio) and carbohydrate-protein neoglycoconjugate vaccine using mass spectrometry (MS) and tandem mass spectrometry (MS/MS). The main objective of the first study was to determine structural changes in snow crab cryptocyanin protein. Accordingly, cryptocyanin was isolated and purified from molting and non molting snow crabs. The purified molting and non molting cryptocyanins were sequenced by using matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS) and collsion induced dissocation tandem mass spectrometry (CID-MS/MS). The structural differences between molting and non-molting cryptocyanin were reported using bottom-up proteomics. The molecular masses of the snow crab during molting and non-molting stages were found to be respectively 67.6 kDa and 68.1 kDa. In the second study, two anti-tumor Thomsen-Friedenreich neoglycoconjugate vaccines were prepared by the Michael addition reaction, and their molecular composition was confirmed by MALDI-TOF-MS analysis. De novo peptide sequencing using electrospray ionization in the positive ion mode mass spectrometry (ESI-MS, + ion mode) and low-energy CID-MS/MS of trypsin digests using a quadrupole-quadrupole-time of flight –hybrid tandem mass spectrometer (QqTOF-MS/MS). The CID-analysis allowed us to identify three glycation sites for the glycoconjugate prepared with a TF: protein ratio of 2:1, and 14 glycation sites for the glycoconjugate prepared with a TF: protein ratio of 8:1. It should be noted that this work represents the only published report for the determination of the exact poistions of the carbohydrate haptens on this unique C-S linked glycoconjugate. In addition, this investigation constitutes a versatile example for the identification of accurate quality control necessary in commercial production of glycoconjugate vaccines. Indeed, the glycopeptides isolated were fully characterized during this work and may well ... |
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