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  Glycomic and sialoproteomic data of gastric carcinoma cells overexpressing ST3GAL4

Mereiter, S., Magalhães, A., Adamczyk, B., Jin, C., Almeida, A., Drici, L., et al. (2016). Glycomic and sialoproteomic data of gastric carcinoma cells overexpressing ST3GAL4. Data in Brief, 7, 814-833. doi:10.1016/j.dib.2016.03.022.

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 Creators:
Mereiter, Stefan, Author
Magalhães, Ana, Author
Adamczyk, Barbara, Author
Jin, Chunsheng, Author
Almeida, Andreia1, Author              
Drici, Lylia, Author
Ibáñez-Vea, Maria, Author
Larsen, Martin R., Author
Kolarich, Daniel1, Author              
Karlsson, Niclas G., Author
Reis, Celso A., Author
Affiliations:
1Daniel Kolarich, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863301              

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Free keywords: N-glycome; O-glycome; Gastric cancer; Sialyltransferase; Sialoproteome; Open Access
 Abstract: Gastric carcinoma MKN45 cells stably transfected with the full-length ST3GAL4 gene were characterised by glycomic and sialoproteomic analysis. Complementary strategies were applied to assess the glycomic alterations induced by ST3GAL4 overexpression. The N-and O-glycome data were generated in two parallel structural analyzes, based on PGC-ESI-MS/MS. Data on glycan structure identification and relative abundance in ST3GAL4 overexpressing cells and respective mock control are presented. The sialoproteomic analysis based on titanium-dioxide enrichment of sialopeptides with subsequent LC-MS/MS identification was performed. This analysis identified 47 proteins with significantly increased sialylation. The data in this article is associated with the research article published in Biochim Biophys Acta “Glycomic analysis of gastric carcinoma cells discloses glycans as modulators of RON receptor tyrosine kinase activation in cancer” [1].

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 Dates: 2016-03-142016
 Publication Status: Published in print
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1016/j.dib.2016.03.022
BibTex Citekey: Mereiter2016
 Degree: -

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Title: Data in Brief
Source Genre: Journal
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Publ. Info: Dordrecht : Elsevier
Pages: - Volume / Issue: 7 Sequence Number: - Start / End Page: 814 - 833 Identifier: ISSN: 2352-3409