Cell-Surface Glyco-Engineering by Exogenous Enzymatic Transfer Using a Bifunctional CMP-Neu5Ac Derivative

J Am Chem Soc. 2017 Sep 27;139(38):13342-13348. doi: 10.1021/jacs.7b05358. Epub 2017 Sep 15.

Abstract

Cell-surface engineering strategies that permit long-lived display of well-defined, functionally active molecules are highly attractive for eliciting desired cellular responses and for understanding biological processes. Current methodologies for the exogenous introduction of synthetic biomolecules often result in short-lived presentations, or require genetic manipulation to facilitate membrane attachment. Herein, we report a cell-surface engineering strategy that is based on the use of a CMP-Neu5Ac derivative that is modified at C-5 by a bifunctional entity composed of a complex synthetic heparan sulfate (HS) oligosaccharide and biotin. It is shown that recombinant ST6GAL1 can readily transfer the modified sialic acid to N-glycans of glycoprotein acceptors of living cells resulting in long-lived display. The HS oligosaccharide is functionally active, can restore protein binding, and allows activation of cell signaling events of HS-deficient cells. The cell-surface engineering methodology can easily be adapted to any cell type and is highly amenable to a wide range of complex biomolecules.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, CD / metabolism*
  • Biotin / metabolism
  • Cell Engineering / methods*
  • Cells, Cultured
  • Cytidine Monophosphate / analogs & derivatives*
  • Cytidine Monophosphate / metabolism
  • Glycoproteins / metabolism
  • Glycosylation
  • Heparitin Sulfate / deficiency
  • Heparitin Sulfate / metabolism
  • Humans
  • Mice
  • Oligosaccharides / metabolism
  • Protein Binding
  • Sialic Acids / metabolism*
  • Sialyltransferases / metabolism*
  • Signal Transduction

Substances

  • Antigens, CD
  • Glycoproteins
  • Oligosaccharides
  • Sialic Acids
  • cytidine-5'-monophosphosialic acid
  • Biotin
  • Heparitin Sulfate
  • Sialyltransferases
  • ST6GAL1 protein, human
  • Cytidine Monophosphate