A lysine-free REC tag system for proximity-biotinylation applications
Protein-protein interaction analysis requires not only the detection of a single protein but also multiple interacting proteins. The proximity-dependent biotin identification (BioID) method using biotin proximity-labelled enzymes is a protein-protein interaction method used in cells and in vivo; however, the detection tags are limited because even the lysine residues of the amino acids in the detection tag are labelled by the enzyme. Herein, we demonstrated a new affinity tag system without lysine residues suitable for use in the BioID method. After immunisation of rabbits with Plasmodium falciparum PfRipr5 protein, 22 anti-PfRipr5 monoclonal antibodies were isolated by ImmunoSpot Array Assay on a Chip, and their binding and specificity were analysed. The results showed that No. 6 anti-PfRipr5 monoclonal antibody had the highest sensitivity and specificity. The epitope was identified to contain one lysine residue; therefore, the mutated epitope, which was replaced with an arginine residue, showed similar binding properties. It was named REC tag for further analysis, and the REC tag was compatible with IB, AlphaScreen, and immunostaining and showed resistance to biotinylation using TurboID in vitro. These results indicate that a new detection tag system could be developed, in which REC tags could be used to detect BioID methods.
Authors
- Eizo Takashima (ORCID: https://orcid.org/0000-0001-9070-8499)
- Tatsuya Sawasaki (ORCID: https://orcid.org/0000-0002-7952-0556)
- Tatsuhiko Ozawa
- Fumiya Soga
- Hikaru Nagaoka (ORCID: https://orcid.org/0000-0003-2167-1754)
- Soh Tokunaga
- Kohdai Yamada (ORCID: https://orcid.org/0009-0001-9695-8445)
- Hiroyuki Takeda
- Hinako Fujisaki
- Hiroyuki Kishi
- Mana Hamada
Institutions
- University of Toyama (JP)
- Ehime University (JP)
Publication Details
- Journal
- Scientific Reports
- Published
- 2026-01-08
- DOI
- https://doi.org/10.1038/s41598-026-35323-w
- Primary Topic
- Biotin and Related Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Agency for Medical Research and Development
- University of Tokushima
- Japan Society for the Promotion of Science