Title : Complete analysis of the glycosylation and disulfide bond pattern of human
beta-hexosaminidase B by MALDI-MS
Abstract :
- beta-hexosaminidase B is an enzyme that is involved in the degradation of glycolipids and glycans in the lysosome
- Mutation in the HEXB gene lead to Sandhoff disease, a glycolipid storage disorder characterized by severe neurodegeneration
- So far, little structural information on the protein is available
- Here, the complete analysis of the disulfide bond pattern of the protein is described for the first time
- Additionally, the structures of the N-glycans are analyzed for the native human protein and for recombinant protein expressed in SF21 cells
- For the analysis of the disulfide bond structure, the protein was proteolytically digested and the resulting peptides were analyzed by MALDI-MS
- The analysis revealed three disulfide bonds (C91-C137; C309-C360; C534-C551) and a free cysteine (C487)
- The analysis of the N-glycosylation was performed by tryptic digestion of the protein , isolation of glycopeptides by lectin chromatography and mass measurement before and after enzymatic deglycosylation
- Carbohydrate structures were calculated from the mass difference between glycosylated and deglycosylated peptide
- For beta-hexosaminidase B from human placenta, four N-glycans were identified and analyzed, whereas the recombinant protein expressed in SF21 cells carried only three glycans
- In both cases the glycosylation belongs to the mannose-core- or high-mannose-type, and some carbohydrate structures are fucosylated
Output (sent_index, trigger,
protein,
sugar,
site):
- 10. carried, , protein, only three glycans, -
- 11. fucosylated, , -, some carbohydrate structures, -
- 8. glycopeptides, , -, -, glycopeptides
- 9. glycosylated, , -, -, peptide
Output(Part-Of) (sent_index,
protein,
site):
*Output_Site_Fusion* (sent_index,
protein,
sugar,
site):