Fluorophore-Conjugated Holliday Junctions for Generating Super-Bright Antibodies and Antibody Fragments

Angew Chem Int Ed Engl. 2015 Sep 28;54(40):11706-10. doi: 10.1002/anie.201505277. Epub 2015 Aug 7.

Abstract

The site-specific modification of proteins with fluorophores can render a protein fluorescent without compromising its function. To avoid self-quenching from multiple fluorophores installed in close proximity, we used Holliday junctions to label proteins site-specifically. Holliday junctions enable modification with multiple fluorophores at reasonably precise spacing. We designed a Holliday junction with three of its four arms modified with a fluorophore of choice and the remaining arm equipped with a dibenzocyclooctyne substituent to render it reactive with an azide-modified fluorescent single-domain antibody fragment or an intact immunoglobulin produced in a sortase-catalyzed reaction. These fluorescent Holliday junctions improve fluorescence yields for both single-domain and full-sized antibodies without deleterious effects on antigen binding.

Keywords: DNA technology; Holiday junctions; antibodies; imaging agents; immunocytochemistry.

MeSH terms

  • Alkynes / chemistry*
  • Antibodies / analysis*
  • Antibodies / chemistry*
  • Azides / chemistry*
  • DNA, Cruciform / chemistry*
  • Fluorescent Dyes / chemistry*

Substances

  • Alkynes
  • Antibodies
  • Azides
  • DNA, Cruciform
  • Fluorescent Dyes