Preparation of Maleimide-Modified Oligonucleotides from the Corresponding Amines Using N‑Methoxycarbonylmaleimide

• Published in: Bioconjugate chemistry 2022-07, Vol.33 (7), p.1254-1260
• Main Authors: Kjærsgaard, Nanna L., Hansen, Rikke A., Gothelf, Kurt V.
• Format: Article
• Language: English
• Subjects: Amines; Bovine serum albumin; Conjugates; Cyclohexane; Deoxyribonucleic acid; DNA; Oligonucleotides; Serum albumin; Solid phases
• ISSN: 1043-1802; 1520-4812
• DOI: 10.1021/acs.bioconjchem.2c00144

Oligonucleotide conjugates constitute a versatile tool for research and bioanalytical purposes. Often, such conjugates are prepared by reaction between a thiol on the protein with a maleimide-modified oligonucleotide. Unlike most other chemical handles the maleimide functionality cannot be introduced directly during the solid-phase oligonucleotide synthesis, and therefore the standard method to introduce the maleimide functionality is to react an amino-modified DNA with a heterobifunctional linker containing an activated ester and a maleimide. Here, we present an alternative method for preparation of maleimide and monobromomaleimide-modified oligonucleotides from the corresponding amine using N-methoxycarbonylmaleimide and N-methoxycarbonylbromomaleimide, respectively. In this method, no additional linker is attached to the oligonucleotide, as the maleimide functionality is formed directly on the existing amine. The maleimide can thereby be positioned close to the oligonucleotide, providing a high degree of control over the final construct. The reaction occurs in 30–60 min under alkaline conditions. Maleimide-modified oligonucleotides prepared in this manner were conjugated to bovine serum albumin, and the reaction shows comparable reactivity to the corresponding oligonucleotide modified using the 4-(N-maleimidomethyl)-cyclohexane-1-carboxylate (SMCC) linker.