A Human Pluripotent Stem Cell Surface N-Glycoproteome Resource Reveals Markers, Extracellular Epitopes, and Drug Targets

Bibliographic Details
Title: A Human Pluripotent Stem Cell Surface N-Glycoproteome Resource Reveals Markers, Extracellular Epitopes, and Drug Targets
Authors: Kenneth R. Boheler, Subarna Bhattacharya, Erin M. Kropp, Sandra Chuppa, Daniel R. Riordon, Damaris Bausch-Fluck, Paul W. Burridge, Joseph C. Wu, Robert P. Wersto, Godfrey Chi Fung Chan, Sridhar Rao, Bernd Wollscheid, Rebekah L. Gundry
Source: Stem Cell Reports, Vol 3, Iss 1, Pp 185-203 (2014)
Publisher Information: Elsevier, 2014.
Publication Year: 2014
Collection: LCC:Medicine (General)
LCC:Biology (General)
Subject Terms: Medicine (General), R5-920, Biology (General), QH301-705.5
More Details: Detailed knowledge of cell-surface proteins for isolating well-defined populations of human pluripotent stem cells (hPSCs) would significantly enhance their characterization and translational potential. Through a chemoproteomic approach, we developed a cell-surface proteome inventory containing 496 N-linked glycoproteins on human embryonic (hESCs) and induced PSCs (hiPSCs). Against a backdrop of human fibroblasts and 50 other cell types, >100 surface proteins of interest for hPSCs were revealed. The >30 positive and negative markers verified here by orthogonal approaches provide experimental justification for the rational selection of pluripotency and lineage markers, epitopes for cell isolation, and reagents for the characterization of putative hiPSC lines. Comparative differences between the chemoproteomic-defined surfaceome and the transcriptome-predicted surfaceome directly led to the discovery that STF-31, a reported GLUT-1 inhibitor, is toxic to hPSCs and efficient for selective elimination of hPSCs from mixed cultures.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2213-6711
Relation: http://www.sciencedirect.com/science/article/pii/S221367111400143X; https://doaj.org/toc/2213-6711
DOI: 10.1016/j.stemcr.2014.05.002
Access URL: https://doaj.org/article/4cb4d4fca3d44ea7ab17c6b73157557c
Accession Number: edsdoj.4cb4d4fca3d44ea7ab17c6b73157557c
Database: Directory of Open Access Journals
More Details
ISSN:22136711
DOI:10.1016/j.stemcr.2014.05.002
Published in:Stem Cell Reports
Language:English