In vitro selection of dye-fluorescence-enhancing peptide aptamer by cDNA display
Although Green Fluorescent Protein (GFP) is useful and most widely used, steric hindrance due to its size and the time required for chromophore formation are complications. However, it is difficult to form chromophores with peptides to reduce the molecular weight. Therefore, we focused on peptides that can become fluorescent by binding to dyes. In this study, a novel dye-fluorescence-enhancing peptide aptamer was selected by the cDNA display method, which was confirmed by the yeast surface display method. This peptide aptamer binds to the non-fluorescent dye QSY®9 and enhances its fluorescence by preventing rotation of its benzene sulfone group. The method described in this paper should enable the development of new cell imaging methods using non-fluorescent dyes and peptides.
Authors
- Naoto Nemoto
- Kenjiro Hanaoka (ORCID: https://orcid.org/0000-0003-0797-4038)
- Mitsuyoshi Ueda (ORCID: https://orcid.org/0000-0003-2268-2391)
- Kouichi Kuroda (ORCID: https://orcid.org/0000-0002-9249-0486)
- Takashi Kubo (ORCID: https://orcid.org/0000-0001-6809-7396)
- Eita Sasaki (ORCID: https://orcid.org/0000-0002-8202-4465)
- Nayab Khaliq
- Tomoki Ouchi
- Tomoyuki Koike
Institutions
- Keio University (JP)
- Kyoto University (JP)
- Kyoto Institute of Technology (JP)
- Saitama University (JP)
Publication Details
- Journal
- Analytical Biochemistry
- Published
- 2024-11-23
- DOI
- https://doi.org/10.1016/j.ab.2024.115722
- Citations
- 1
- Primary Topic
- Advanced biosensing and bioanalysis techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.23
Funders
- Japan Science and Technology Corporation
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency