Affiliation:
1. Department of Molecular Medicine The Scripps Research Institute La Jolla CA 92037 USA
2. Department of Chemistry The Scripps Research Institute La Jolla CA 92037 USA.
3. Department of Biology California Institute for Biomedical Research (Calibr) The Scripps Research Institute La Jolla CA 92037 USA.
4. Department of Biochemistry and Molecular Biology University of Georgia Athens GA 30602
Abstract
AbstractTruncated mucin‐type O‐glycans, such as Tn‐associated antigens, are aberrantly expressed biomarkers of cancer, but remain challenging to target. Reactive antibodies to these antigens either lack high affinity or are prone to antigen escape. Here, we have developed a robust chemoenzymatic strategy for the global labeling of Tn‐associated antigens, i. e. Tn (GalNAcα‐O‐Ser/Thr), Thomsen‐Friedenreich (Galβ1‐3GalNAcα‐O‐Ser/Thr, TF) and STF (Neu5Acα2‐3Galβ1‐3GalNAcα‐O‐Ser/Thr, STF) antigens, in human whole blood with high efficiency and selectivity. This method relies on the use of the O‐glycan sialyltransferase ST6GalNAc1 to transfer a sialic acid‐functionalized adaptor to the GalNAc residue of these antigens. By tagging, the adaptor functionalized antigens can be easily targeted by customized strategies such as, but not limited to, chimeric antigen receptor T‐Cells (CAR‐T). We expect this tagging system to find broad applications in cancer diagnostics and targeting in combination with established strategies.
Funder
National Institutes of Health
Cited by
2 articles.
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