4.7 Article

Site-Specific Dual Antibody Conjugation via Engineered Cysteine and Selenocysteine Residues

Journal

BIOCONJUGATE CHEMISTRY
Volume 26, Issue 11, Pages 2243-2248

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.bioconjchem.5b00244

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Funding

  1. National Institutes of Health [U01 CA174844, R01 CA181258]
  2. Lymphoma Research Foundation
  3. Klorfine Foundation

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Site-specific conjugation technologies enable the production of homogeneous antibody drug conjugates (ADCs) with improved therapeutic indices compared to conventional ADCs. However, current site-specific conjugation methods can only attach one type of drug to a single antibody. Given the emergence of acquired resistance to current ADCs, arming single antibodies with different drugs may provide an attractive option in the development of next-generation ADCs. Here, we describe a site-specific dual conjugation strategy as a platform for dual warhead ADCs.

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