Engineered Fragments of the PSMA-Specific 5D3 Antibody and Their Functional Characterization
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F20%3A00539375" target="_blank" >RIV/61388963:_____/20:00539375 - isvavai.cz</a>
Alternative codes found
RIV/86652036:_____/20:00539375
Result on the web
<a href="https://www.mdpi.com/1422-0067/21/18/6672" target="_blank" >https://www.mdpi.com/1422-0067/21/18/6672</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/ijms21186672" target="_blank" >10.3390/ijms21186672</a>
Alternative languages
Result language
angličtina
Original language name
Engineered Fragments of the PSMA-Specific 5D3 Antibody and Their Functional Characterization
Original language description
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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10406 - Analytical chemistry
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Molecular Sciences
ISSN
1422-0067
e-ISSN
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Volume of the periodical
21
Issue of the periodical within the volume
18
Country of publishing house
CH - SWITZERLAND
Number of pages
21
Pages from-to
6672
UT code for WoS article
000582019100001
EID of the result in the Scopus database
2-s2.0-85090585899