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Description
Spontaneous Isopeptide Bond Formation as a Powerful Tool for Engineering Site-Specific Antibody-Drug Conjugates
[DOI] [PubMed] [Google Scholar] 117.Marty L., Siala W., Schwarzlander M., Fricker M.D., Wirtz M., Sweetlove L.J., Meyer Y., Meyer A.J., Reichheld J.P., Hell R
et al (2014) Biomacromolecules
In one preferred embodiment of the invention, the ligand is conjugated or synthesized via the N-terminal amino acid residue, i.e
C.PerezD.RedaelliC.GloorB.TrentzO.et al (2001)
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