Cell surface glycoproteomic analysis of prostate cancer-derived PC-3 cells.
Abstract
Most clinically approved biomarkers of cancer are glycoproteins, and those residing
on the cell surface are of particular interest in biotherapeutics. We report a method
for selective labeling, affinity enrichment, and identification of cell-surface glycoproteins.
PC-3 cells and primary human prostate cancer tissue were treated with peracetylated
N-azidoacetylgalactosamine, resulting in metabolic labeling of cell surface glycans
with the azidosugar. We used mass spectrometry to identify over 70 cell surface glycoproteins
and biochemically validated CD146 and integrin beta-4, both of which are known to
promote metastatic behavior. These results establish cell-surface glycoproteomics
as an effective technique for discovery of cancer biomarkers.
Type
Journal articleSubject
Cell Line, TumorHumans
Prostatic Neoplasms
Carbohydrates
Proteome
Electrophoresis, Polyacrylamide Gel
Male
Mass Spectrometry
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https://hdl.handle.net/10161/19699Published Version (Please cite this version)
10.1016/j.bmcl.2011.05.045Publication Info
Hubbard, Sarah C; Boyce, Michael; McVaugh, Cheryl T; Peehl, Donna M; & Bertozzi, Carolyn
R (2011). Cell surface glycoproteomic analysis of prostate cancer-derived PC-3 cells. Bioorganic & medicinal chemistry letters, 21(17). pp. 4945-4950. 10.1016/j.bmcl.2011.05.045. Retrieved from https://hdl.handle.net/10161/19699.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Michael Scott Boyce
Associate Professor of Biochemistry
The Boyce Lab studies mammalian cell signaling through protein glycosylation. For
the latest news, project information and publications from our group, please visit
our web site at http://www.boycelab.org or follow us on Twitter at https://twitter.com/BoyceLab.

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