Expression, purification, characterization, and cytotoxic evaluation of the ML1-STxB fusion protein.


Journal

Archives of microbiology
ISSN: 1432-072X
Titre abrégé: Arch Microbiol
Pays: Germany
ID NLM: 0410427

Informations de publication

Date de publication:
06 May 2023
Historique:
received: 30 01 2023
accepted: 20 04 2023
revised: 18 04 2023
medline: 8 5 2023
pubmed: 6 5 2023
entrez: 6 5 2023
Statut: epublish

Résumé

Targeted delivery of a toxin substance to cancer cells is one of the most recent cancer treatment options. Mistletoe Lectin-1 (ML1) in Viscum album L. is a Ribosome-inactivating proteins with anticancer properties. Therefore, it appears that a recombinant protein with selective permeability can be generated by fusing ML1 protein with Shiga toxin B, which can bind to Gb3 receptor that is abundantly expressed on cancer cells. In this study, we sought to produce and purify a fusion protein containing ML1 fused to STxB and evaluate its cytotoxic activities. The ML1-STxB fusion protein coding sequence was cloned into the pET28a plasmid, then was transformed into E. coli BL21-DE3 cells. Following induction of protein expression, Ni-NTA affinity chromatography was used to purify the protein. Using SDS-PAGE and western blotting, the expression and purification processes were validated. On the SkBr3 cell line, the cytotoxic effects of the recombinant proteins were evaluated. On SDS-PAGE and western blotting membrane, analysis of purified proteins revealed a band of approximately 41 kDa for rML1-STxB. Ultimately, statistical analysis demonstrated that rML1-STxB exerted significant cytotoxic effects on SkBr3 cells at 18.09 and 22.52 ng/L. The production, purification, and encapsulation of rML1-STxB fusion protein with potential cancer cell-specific toxicity were successful. However, additional research must be conducted on the cytotoxic effects of this fusion protein on other malignant cell lines and in vivo cancer models.

Identifiants

pubmed: 37148384
doi: 10.1007/s00203-023-03563-3
pii: 10.1007/s00203-023-03563-3
doi:

Substances chimiques

Lectins 0
Recombinant Proteins 0
Antineoplastic Agents 0
Biological Products 0
Recombinant Fusion Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

220

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Mohammad Hasan Yousefi (MH)

Department of Cellular and Molecular Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran.

Hamed Afkhami (H)

Department of Medical Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.

Atefeh Akbari (A)

Faculty of Pharmacy, Lorestan University of Medical Sciences, Khorramabad, Iran.

Hossein Honari (H)

Department of Cellular and Molecular Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran. honari.hosein@gmail.com.

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Classifications MeSH