4.8 Article

Galactose Oxidase Enables Modular Assembly of Conjugates from Native Antibodies with High Drug-to-Antibody Ratios**

期刊

CHEMSUSCHEM
卷 15, 期 9, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202102592

关键词

antibodies; antibody-drug conjugates; biocatalysis; glycoengineering; medicinal chemistry

资金

  1. EPSRC [EP/S005226/1, BB/M017702/1]
  2. BBSRC [EP/S005226/1, BB/M017702/1]
  3. AstraZeneca [EP/S005226/1, BB/M017702/1]
  4. EPSRC [EP/S005226/1] Funding Source: UKRI

向作者/读者索取更多资源

A glycoengineering methodology was developed to generate antibody drug conjugates with high drug loading by combining enzymatic galactosylation and oxidation with biorthogonal tandem Knoevenagel-Michael addition chemistry.
The potential of antibody conjugates with high drug loading in anticancer therapy has recently been highlighted by the approval of Trastuzumab deruxtecan and Sacituzumab govitecan. These biopharmaceutical approaches have spurred interest in bioconjugation strategies with high and defined degrees of drug-to-antibody ratio (DAR), in particular on native antibodies. Here, a glycoengineering methodology was developed to generate antibody drug conjugates with DAR of up to eight, by combining highly selective enzymatic galactosylation and oxidation with biorthogonal tandem Knoevenagel-Michael addition chemistry. This four-step approach offers a selective route to conjugates from native antibodies with high drug loading, and thus illustrates how biocatalysis can be used for the generation of biopharmaceuticals using mild reaction conditions.

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