Preparation of Protein Conjugates via Homobifunctional Diselenoester Cross-Linker

Org Lett. 2016 Nov 18;18(22):5796-5799. doi: 10.1021/acs.orglett.6b02568. Epub 2016 Nov 4.

Abstract

Adipic acid diselenoester was developed as an efficient cross-linker for covalent protein conjugation with a variety of small molecular haptens, including mono- and disaccharides, peptide, fluorescence dye, and nicotine. Compared to the counterparts of N-hydroxysuccinimide (NHS) and p-nitrophenyl (PNP) linkers, the diselenoester linker demonstrates improved balance between reactivity and stability and coupling of haptens to proteins under mild conditions with high incorporation efficiency.

Publication types

  • Historical Article
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipates / chemical synthesis
  • Adipates / chemistry*
  • Cross-Linking Reagents / chemical synthesis
  • Cross-Linking Reagents / chemistry*
  • Haptens / chemistry*
  • History, 20th Century
  • Organoselenium Compounds / chemical synthesis
  • Organoselenium Compounds / chemistry*
  • Ovalbumin / chemistry*
  • Serum Albumin, Bovine / chemistry*
  • Vaccines, Synthetic / chemistry

Substances

  • Adipates
  • Cross-Linking Reagents
  • Haptens
  • Organoselenium Compounds
  • Vaccines, Synthetic
  • Serum Albumin, Bovine
  • adipic acid
  • Ovalbumin