Open Access
Open access
Molecules, volume 25, issue 24, pages 5784

Polypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen

Zyk Nikolay Y 1
Nimenko Ekaterina A. 1
Garanina A. S. 1, 2
Petrov Rostislav A 1
Grishin Yuri K. 1
Zyk Nikolay V. 1
Majouga Alexander G. 1, 2, 4
Publication typeJournal Article
Publication date2020-12-08
Journal: Molecules
Quartile SCImago
Q1
Quartile WOS
Q2
Impact factor4.6
ISSN14203049
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract

A strategy for stereoselective synthesis of molecular platform for targeted delivery of bimodal therapeutic or theranostic agents to the prostate-specific membrane antigen (PSMA) receptor was developed. The proposed platform contains a urea-based, PSMA-targeting Glu-Urea-Lys (EuK) fragment as a vector moiety and tripeptide linker with terminal amide and azide groups for subsequent addition of two different therapeutic and diagnostic agents. The optimal method for this molecular platform synthesis includes (a) solid-phase assembly of the polypeptide linker, (b) coupling of this linker with the vector fragment, (c) attachment of 3-aminopropylazide, and (d) amide and carboxylic groups deprotection. A bimodal theranostic conjugate of the proposed platform with a cytostatic drug (docetaxel) and a fluorescent label (Sulfo-Cy5) was synthesized to demonstrate its possible sequential conjugation with different functional molecules.

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GOST Copy
Petrov S. B. et al. Polypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen // Molecules. 2020. Vol. 25. No. 24. p. 5784.
GOST all authors (up to 50) Copy
Petrov S. B., Machulkin A. E., Uspenskaya A. A., Zyk N. Y., Nimenko E. A., Garanina A. S., Petrov R. A., Polshakov V. I., Grishin Y. K., Roznyatovsky V. A., Zyk N. V., Majouga A. G., Beloglazkina E. K. Polypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen // Molecules. 2020. Vol. 25. No. 24. p. 5784.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3390/molecules25245784
UR - https://doi.org/10.3390%2Fmolecules25245784
TI - Polypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen
T2 - Molecules
AU - Uspenskaya, Anastasia A
AU - Zyk, Nikolay Y
AU - Nimenko, Ekaterina A.
AU - Grishin, Yuri K.
AU - Zyk, Nikolay V.
AU - Majouga, Alexander G.
AU - Petrov, Stanislav B.
AU - Machulkin, Aleksei E.
AU - Garanina, A. S.
AU - Petrov, Rostislav A
AU - Polshakov, Vladimir I.
AU - Roznyatovsky, Vitaly A
AU - Beloglazkina, Elena K.
PY - 2020
DA - 2020/12/08 00:00:00
PB - Multidisciplinary Digital Publishing Institute (MDPI)
SP - 5784
IS - 24
VL - 25
PMID - 33302417
SN - 1420-3049
ER -
BibTex |
Cite this
BibTex Copy
@article{2020_Petrov,
author = {Anastasia A Uspenskaya and Nikolay Y Zyk and Ekaterina A. Nimenko and Yuri K. Grishin and Nikolay V. Zyk and Alexander G. Majouga and Stanislav B. Petrov and Aleksei E. Machulkin and A. S. Garanina and Rostislav A Petrov and Vladimir I. Polshakov and Vitaly A Roznyatovsky and Elena K. Beloglazkina},
title = {Polypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen},
journal = {Molecules},
year = {2020},
volume = {25},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
month = {dec},
url = {https://doi.org/10.3390%2Fmolecules25245784},
number = {24},
pages = {5784},
doi = {10.3390/molecules25245784}
}
MLA
Cite this
MLA Copy
Petrov, Stanislav B., et al. ā€œPolypeptide-Based Molecular Platform and Its Docetaxel/Sulfo-Cy5-Containing Conjugate for Targeted Delivery to Prostate Specific Membrane Antigen.ā€ Molecules, vol. 25, no. 24, Dec. 2020, p. 5784. https://doi.org/10.3390%2Fmolecules25245784.
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