A novel approach to chemical microarray using ketone-modified macromolecular scaffolds: Application in micro cell-adhesion assay

Qingchai Xu, Suzanne Miyamoto, Kit Lam

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

This paper describes a novel strategy for the preparation of chemical microarrays using macro-molecular scaffolds. The macromolecular scaffolds are first functionalized with ketone groups and compounds of interest containing an aminooxy group are conjugated onto the ketone-modified scaffolds through a chemoselective oxime ligation. The conjugate mixtures are then spotted directly onto a plastic or glass surface to form compound microarrays. Because a constant amount of scaffold is used in the presence of excess compound in the ligation reaction, the amount of compound actually immobilized per microarray spot is constant and dependent on the scaffold concentration. Using this approach, 60 different peptides were ligated to human serum albumin or agarose scaffolds, and the peptide conjugates subsequently printed on glass or polystyrene surface to form microarrays. These peptide microarrays were subsequently evaluated and optimized for binding of Jurkat leukemic cancer cells.

Original languageEnglish (US)
Pages (from-to)301-310
Number of pages10
JournalMolecular Diversity
Volume8
Issue number3
DOIs
StatePublished - 2004

Fingerprint

Cell adhesion
Scaffolds (biology)
Microarrays
Ketones
Cell Adhesion
Scaffolds
ketones
peptides
Assays
adhesion
Peptides
Glass
Ligation
cells
Public Opinion
Oximes
glass
Polystyrenes
albumins
Serum Albumin

Keywords

  • chemical microarray
  • ketone-modified scaffold
  • peptide microarray
  • peptide-agarose conjugate
  • peptide-HSA conjugate

ASJC Scopus subject areas

  • Chemistry (miscellaneous)
  • Drug Discovery
  • Organic Chemistry

Cite this

A novel approach to chemical microarray using ketone-modified macromolecular scaffolds : Application in micro cell-adhesion assay. / Xu, Qingchai; Miyamoto, Suzanne; Lam, Kit.

In: Molecular Diversity, Vol. 8, No. 3, 2004, p. 301-310.

Research output: Contribution to journalArticle

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