Introduction of Carbonyl Groups into Antibodies

Author:

Gulyak Evgeny L.1,Alferova Vera A.1ORCID,Korshun Vladimir A.1ORCID,Sapozhnikova Ksenia A.1ORCID

Affiliation:

1. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, 117997 Moscow, Russia

Abstract

Antibodies and their derivatives (scFv, Fabs, etc.) represent a unique class of biomolecules that combine selectivity with the ability to target drug delivery. Currently, one of the most promising endeavors in this field is the development of molecular diagnostic tools and antibody-based therapeutic agents, including antibody–drug conjugates (ADCs). To meet this challenge, it is imperative to advance methods for modifying antibodies. A particularly promising strategy involves the introduction of carbonyl groups into the antibody that are amenable to further modification by biorthogonal reactions, namely aliphatic, aromatic, and α-oxo aldehydes, as well as aliphatic and aryl–alkyl ketones. In this review, we summarize the preparation methods and applications of site-specific antibody conjugates that are synthesized using this approach.

Funder

Ministry of Science and Higher Education of the Russian Federation

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Reference263 articles.

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3. Narain, R. (2014). Chemistry of Bioconjugates: Synthesis, Characterization, and Biomedical Applications, Wiley. [1st ed.].

4. Hermanson, G.T. (2013). Bioconjugate Techniques, Elsevier.

5. Algar, W.R., Dawson, P., and Medintz, I.L. (2017). Chemoselective and Bioorthogonal Ligation Reactions, Wiley-VCH.

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