Modular Nanotransporters Containing Anti-PSMA Nanobodies Are Able to Penetrate into the Nuclei of Prostate Cancer Cells

Polypeptide modular nanotransporters (MNTs) were engineered as a targeted delivery platform for prostate cancer cells. The constructs integrate a ligand module to facilitate specific cellular binding and internalization, and a nuclear localization signal (NLS) to enable subsequent nuclear translocation. Two distinct ligand modules were utilized: (a) a nanobody targeting prostate-specific membrane antigen (anti-PSMA) and (b) a gastrin-releasing peptide (GRP) fragment targeting the GRP receptor (GRPR). It was shown that all modules within MNT-antiPSMA and MNT-GRP retained their functional properties. The MNT-antiPSMA construct demonstrated the capacity to accumulate specifically in the nuclei of prostate cancer cells with both low and high PSMA expression. Conversely, MNT-GRP exhibited selective nuclear entry exclusively in cells characterized by high GRPR expression.

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Journal
Doklady Biochemistry and Biophysics
Published
2026-04-20
DOI
https://doi.org/10.1134/s1607672925601908
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
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article

Modular Nanotransporters Containing Anti-PSMA Nanobodies Are Able to Penetrate into the Nuclei of Prostate Cancer Cells

Г. П. Георгиев, Y. V. Khramtsov, A. V. Ulasov, T. N. Lupanova et al.
Doklady Biochemistry and Biophysics
Nanoparticle-Based Drug Delivery
article

Modular Nanotransporters Containing Anti-PSMA Nanobodies Are Able to Penetrate into the Nuclei of Prostate Cancer Cells

Г. П. Георгиев, Y. V. Khramtsov, A. V. Ulasov, T. N. Lupanova, A. S. Sobolev, A. A. Rosenkranz, T. A. Slastnikova
article en

Abstract

Polypeptide modular nanotransporters (MNTs) were engineered as a targeted delivery platform for prostate cancer cells. The constructs integrate a ligand module to facilitate specific cellular binding and internalization, and a nuclear localization signal (NLS) to enable subsequent nuclear translocation. Two distinct ligand modules were utilized: (a) a nanobody targeting prostate-specific membrane antigen (anti-PSMA) and (b) a gastrin-releasing peptide (GRP) fragment targeting the GRP receptor (GRPR). It was shown that all modules within MNT-antiPSMA and MNT-GRP retained their functional properties. The MNT-antiPSMA construct demonstrated the capacity to accumulate specifically in the nuclei of prostate cancer cells with both low and high PSMA expression. Conversely, MNT-GRP exhibited selective nuclear entry exclusively in cells characterized by high GRPR expression.

Doklady Biochemistry and Biophysics
Lomonosov Moscow State University (RU), Institute of Gene Biology (RU), Yandex (Russia) (RU)
Good health and well-being
Openalex Percentile: Top 9%
Nanoparticle-Based Drug Delivery
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