The development of chemical strategies for decorating cells with defined carbohydrate epitopes would greatly facilitate studies of carbohydrate-mediated cell surface interactions. This report describes a general strategy for engineering the display of chemically defined oligosaccharides on cell surfaces that combines the concepts of metabolic engineering and selective chemical reactivity. Using a recently described method (Mahal, L. K., Yarema, K. J., and Bertozzi, C. R. (1997) Science 276, 1125-1128), we delivered a uniquely reactive ketone group to endogenous cell surface sialic acid residues by treating cells with the ketone-bearing metabolic precursor N-levulinoylmannosamine (ManLev). The ketone undergoes highly selective condensation reactions with complementary nucleophiles such as aminooxy and hydrazide groups. The detailed quantitative parameters of ManLev metabolism in human and nonhuman-derived cell lines were determined to establish a foundation for the modification of cell surfaces with novel epitopes at defined cell-surface densities. Ketones within the glycoconjugates on ManLev-treated cells were then reacted with synthetic aminooxy and hydrazide-functionalized carbohydrates. The remodeled cells were endowed with novel lectin binding profiles as determined by flow cytometry analysis. The simplicity and generality of this method make it well suited for use in the study of carbohydrate-mediated cell surface interactions.It has been known for several decades that the cell surface is richly decorated with a dense covering of complex oligosaccharides. Even before many of the specific biological functions of these carbohydrates were elucidated, it was apparent that remodeling the molecular landscape of the cell surface transformed the behavior of cells (1, 2). The discovery of their participation in cell-cell recognition events has brought cell surface glycoconjugates to the forefront of biological research in recent years. Numerous cell surface oligosaccharides have been sequenced and their interactions with receptors on opposing cells are understood in some molecular detail (3-7). Nevertheless, the interactions of cell surface oligosaccharides with protein receptors in solution and on opposing cells remain difficult to study at the molecular level in comparison to protein-protein interactions on cell surfaces.The lag in carbohydrate research can be attributed, in part, to the difficulty in controlling the presentation of well defined carbohydrate epitopes on cell surfaces (for a perspective, see Ref. 8). While cell surface oligosaccharide structures can be conservatively altered by the introduction, overexpression, or deletion of genes encoding specific glycosyltransferases (9 -17), the complexities of oligosaccharide biosynthesis impose some limitations on the use of genetic methods for modulating the structures of cell surface oligosaccharides. As a consequence, alternative methods for decorating cells with chemically defined oligosaccharides are the subject of much recent attention (18).Owing to adv...