Abstract
The modification of
lysine residues with acylating agents has represented a ubiquitous approach to
the construction of antibody conjugates, with the resulting amide bonds being
robustly stable and clinically validated. However, the conjugates are highly
heterogeneous, due to the presence of numerous lysines on the surface of the
protein, and greater control of the sites of conjugation are keenly sought. Here we present a novel approach to achieve
the targeted modification of lysines distal to an antibody fragment’s binding
site, using a disulfide bond as a temporary ‘hook’ to deliver the acylating
agent. This cysteine-to-lysine transfer (CLT) methodology offers greatly
improved homogeneity of lysine conjugates, whilst retaining the advantages
offered by the formation of amide linkages.
Supplementary materials
Title
SI Cysteine-To-Lysine Transfer Antibody Fragment Conjugation
Description
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