| Literature DB >> 28330604 |
Xiuling Li1, Christopher G Nelson2, Rajesh R Nair3, Lori Hazlehurst3, Tina Moroni4, Pablo Martinez-Acedo4, Alex R Nanna1, David Hymel2, Terrence R Burke2, Christoph Rader5.
Abstract
Selenomabs are engineered monoclonal antibodies with one or more translationally incorporated selenocysteine residues. The unique reactivity of the selenol group of selenocysteine permits site-specific conjugation of drugs. Compared with other natural and unnatural amino acid and carbohydrate residues that have been used for the generation of site-specific antibody-drug conjugates, selenocysteine is particularly reactive, permitting fast, single-step, and efficient reactions under near physiological conditions. Using a tailored conjugation chemistry, we generated highly stable selenomab-drug conjugates and demonstrated their potency and selectivity in vitro and in vivo. These site-specific antibody-drug conjugates built on a selenocysteine interface revealed broad therapeutic utility in liquid and solid malignancy models.Entities:
Keywords: antibody-drug conjugates; cancer therapy; selenocysteine; site-specific conjugation
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Year: 2017 PMID: 28330604 PMCID: PMC5400723 DOI: 10.1016/j.chembiol.2017.02.012
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116