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Development of a Quenchbody for the Detection and Imaging of the Cancer-Related Tight-Junction-Associated Membrane Protein Claudin.
Jeong, Hee-Jin; Kawamura, Takuya; Iida, Manami; Kawahigashi, Yumi; Takigawa, Mutsumi; Ohmuro-Matsuyama, Yuki; Chung, Chan-I; Dong, Jinhua; Kondoh, Masuo; Ueda, Hiroshi.
Afiliación
  • Jeong HJ; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology , 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
  • Kawamura T; Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo , 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
  • Iida M; Graduate School of Pharmaceutical Sciences, Osaka University , Suita, Osaka 565-0871, Japan.
  • Kawahigashi Y; Graduate School of Pharmaceutical Sciences, Osaka University , Suita, Osaka 565-0871, Japan.
  • Takigawa M; Graduate School of Pharmaceutical Sciences, Osaka University , Suita, Osaka 565-0871, Japan.
  • Ohmuro-Matsuyama Y; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology , 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
  • Chung CI; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology , 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
  • Dong J; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology , 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
  • Kondoh M; Key Laboratory of Biological Medicine in Universities of Shandong Province, School of Bioscience and Technology, Weifang Medical University , Weifang, Shandong 261053, P.R. China.
  • Ueda H; Graduate School of Pharmaceutical Sciences, Osaka University , Suita, Osaka 565-0871, Japan.
Anal Chem ; 89(20): 10783-10789, 2017 10 17.
Article en En | MEDLINE | ID: mdl-28972746
Claudins (CLs) are membrane proteins found in tight junctions and play a major role in establishing the intercellular barrier. However, some CLs are abnormally overexpressed on tumor cells and are valid clinical biomarkers for cancer diagnosis. Here, we constructed antibody Fab fragment-based Quenchbodies (Q-bodies) as effective and reliable fluorescent sensors for detecting and visualizing CLs on live tumor cells. The variable region genes for anti-CL1 and anti-CL4 antibodies were used to express recombinant Fab fragments, and clones recognizing CL4 with high affinity were selected for making Q-bodies. When two fluorescent dyes were conjugated to the N-terminal tags attached to the Fab, the fluorescent signal was significantly increased after adding nanomolar-levels of purified CL4. Moreover, addition of the Q-body to CL4-expressing cells including CL4-positive cancer cells led to a clear fluorescence signal with low background, even without washing steps. Our findings suggested that such Q-bodies would serve as a potent tool for specifically illuminating membrane targets expressed on cancer cells, both in vitro and in vivo.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos Fab de Inmunoglobulinas / Microscopía Confocal / Claudinas Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anal Chem Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos Fab de Inmunoglobulinas / Microscopía Confocal / Claudinas Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anal Chem Año: 2017 Tipo del documento: Article País de afiliación: Japón
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