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A high-throughput O-glycopeptide discovery platform for seromic profiling.


ABSTRACT: Biomarker microarrays are becoming valuable tools for serological screening of disease-associated autoantibodies. Post-translational modifications (PTMs) such as glycosylation extend the range of protein function, and a variety of glycosylated proteins are known to be altered in disease progression. Here, we have developed a synthetic screening microarray platform for facile display of O-glycosylated peptides (O-PTMs). By introduction of a capping step during chemical solid-phase glycopeptide synthesis, selective enrichment of N-terminal glycopeptide end products was achieved on an amine-reactive hydrogel-coated microarray glass surface, allowing high-throughput display of large numbers of glycopeptides. Utilizing a repertoire of recombinant glycosyltransferases enabled further diversification of the array libraries in situ and display of a new level of potential biomarker candidates for serological screening. As proof-of-concept, we have demonstrated that MUC1 glycopeptides could be assembled and used to detect autoantibodies in vaccine-induced disease-free breast cancer patients and in patients with confirmed disease at time of diagnosis.

SUBMITTER: Blixt O 

PROVIDER: S-EPMC3001163 | biostudies-other | 2010 Oct

REPOSITORIES: biostudies-other

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A high-throughput O-glycopeptide discovery platform for seromic profiling.

Blixt Ola O   Cló Emiliano E   Nudelman Aaron S AS   Sørensen Kasper Kildegaard KK   Clausen Thomas T   Wandall Hans H HH   Livingston Philip O PO   Clausen Henrik H   Jensen Knud J KJ  

Journal of proteome research 20101001 10


Biomarker microarrays are becoming valuable tools for serological screening of disease-associated autoantibodies. Post-translational modifications (PTMs) such as glycosylation extend the range of protein function, and a variety of glycosylated proteins are known to be altered in disease progression. Here, we have developed a synthetic screening microarray platform for facile display of O-glycosylated peptides (O-PTMs). By introduction of a capping step during chemical solid-phase glycopeptide sy  ...[more]

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