Recombinant humanized Fab fragments targeting the CFC domain of human Cripto-1.


Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
21 Dec 2023
Historique:
received: 24 10 2023
revised: 19 12 2023
accepted: 20 12 2023
medline: 28 12 2023
pubmed: 28 12 2023
entrez: 27 12 2023
Statut: aheadofprint

Résumé

In the era of immunotherapy, the targeting of disease-specific biomarkers goes hand in hand with the development of highly selective antibody-based reagents having optimal pharmacological/toxicological profiles. One interesting and debated biomaker for several types of cancers is the onco-fetal protein Cripto-1 that is selectively expressed in many solid tumours and has been actively investigated as potential theranostic target. Starting from previously described anti-CFC/Cripto-1 murine monoclonal antibodies, we have moved forward to prepare the humanized recombinant Fabs which have been engineered so as to bear an MTGase site useful for a one-step site-specific labelling. The purified and bioconjugated molecules have been extensively characterized and tested on Cripto-1-positive cancer cells through in vitro binding assays. These recombinant Fab fragments recognize the target antigen in its native form on intact cells suggesting that they can be further developed as reagents for detecting Cripto-1 in theranostic settings.

Identifiants

pubmed: 38150919
pii: S0006-291X(23)01511-5
doi: 10.1016/j.bbrc.2023.149417
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149417

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: MENOTTI RUVO reports financial support was provided by Italy Ministry of University. MENOTTI RUVO reports financial support was provided by Campania Region. Maria Cantile, Riccardo Sanna reports financial support was provided by Italy Ministry of University. Maria Cantile and Riccardo Sanna are employees of BIOVIIIx srl.

Auteurs

Annamaria Sandomenico (A)

Institute of Biostructures and Bioimaging, CNR, Via P. Castellino, 111, 80131, Napoli, Italy. Electronic address: annamaria.sandomenico@cnr.it.

Fabio Selis (F)

BIOVIIIX, via B. Brin 59c, Napoli, Italy.

Jwala P Sivaccumar (JP)

Institute of Biostructures and Bioimaging, CNR, Via P. Castellino, 111, 80131, Napoli, Italy.

PierPaolo Olimpieri (P)

Department of Physics, Sapienza University, 00184, Rome, Italy.

Emanuela Iaccarino (E)

Institute of Biostructures and Bioimaging, CNR, Via P. Castellino, 111, 80131, Napoli, Italy.

Valeria Cicatiello (V)

Institute of Genetics and Biophysics Adriano Buzzati-Traverso, CNR, Via P. Castellino, 111, 80131, Napoli, Italy.

Maria Cantile (M)

BIOVIIIX, via B. Brin 59c, Napoli, Italy.

Riccardo Sanna (R)

BIOVIIIX, via B. Brin 59c, Napoli, Italy.

Antonio Leonardi (A)

Department of Molecular Medicine and Medical Biotechnology, Italy.

Sandro De Falco (S)

Institute of Genetics and Biophysics Adriano Buzzati-Traverso, CNR, Via P. Castellino, 111, 80131, Napoli, Italy.

Menotti Ruvo (M)

Institute of Biostructures and Bioimaging, CNR, Via P. Castellino, 111, 80131, Napoli, Italy. Electronic address: menotti.ruvo@unina.it.

Classifications MeSH