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Engineered Fragments of the PSMA-Specific 5D3 Antibody and Their Functional Characterization
Z. Novakova, N. Belousova, CA. Foss, B. Havlinova, M. Gresova, G. Das, A. Lisok, A. Prada, M. Barinkova, M. Hubalek, MG. Pomper, C. Barinka
Language English Country Switzerland
Document type Journal Article
Grant support
LTAUSA18196
Ministry of education youth and sports, Czech Republic
NLK
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PubMed
32932591
DOI
10.3390/ijms21186672
Knihovny.cz E-resources
- MeSH
- Antigens, Surface immunology MeSH
- Cell Line MeSH
- PC-3 Cells MeSH
- Fluorescence MeSH
- Glutamate Carboxypeptidase II immunology MeSH
- Insecta MeSH
- Single-Chain Antibodies immunology MeSH
- Humans MeSH
- Antibodies, Monoclonal immunology MeSH
- Mice, Nude MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Prostatic Neoplasms immunology MeSH
- Recombinant Proteins immunology MeSH
- Xenograft Model Antitumor Assays methods MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Prostate-Specific Membrane Antigen (PSMA) is an established biomarker for the imaging and experimental therapy of prostate cancer (PCa), as it is strongly upregulated in high-grade primary, androgen-independent, and metastatic lesions. Here, we report on the development and functional characterization of recombinant single-chain Fv (scFv) and Fab fragments derived from the 5D3 PSMA-specific monoclonal antibody (mAb). These fragments were engineered, heterologously expressed in insect S2 cells, and purified to homogeneity with yields up to 20 mg/L. In vitro assays including ELISA, immunofluorescence and flow cytometry, revealed that the fragments retain the nanomolar affinity and single target specificity of the parent 5D3 antibody. Importantly, using a murine xenograft model of PCa, we verified the suitability of fluorescently labeled fragments for in vivo imaging of PSMA-positive tumors and compared their pharmacokinetics and tissue distribution to the parent mAb. Collectively, our data provide an experimental basis for the further development of 5D3 recombinant fragments for future clinical use.
References provided by Crossref.org
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