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Updated: Mar 6, 2026

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Optimisation of the dibromomaleimide (DBM) platform for native antibody conjugation by accelerated post-conjugation
Maurício Morais1, João P M Nunes1, Kersti Karu1
1Department of Chemistry, UCL, 20 Gordon St, London, UK WC1H 0AJ. j.r.baker@ucl.ac.uk v.chudasama@ucl.ac.uk.
Abstract:
Disulfide bridging offers a convenient approach to generate site-selective antibody conjugates from native antibodies. To optimise the reagents available to achieve this strategy, we describe here the use of dibromomaleimides designed to undergo accelerated post-conjugation hydrolysis. Conjugation and hydrolysis, which serve to 'lock' the conjugates as robustly stable maleamic acids, is achieved in just over 1 h. This dramatic acceleration is also shown to infer significant improvements in homogeneity, as demonstrated by mass spectrometry analysis.

