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Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties

[Image: see text] Conjugates based on cell-penetrating peptides (CPPs) are scientifically relevant owing to their structural complexity; their ability to enter cells and deliver drugs, labels, antioxidants, bioactive compounds, or DNA fragments; and, consequently, their potential for application in...

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Autores principales: Okuda-Shinagawa, Nancy M., Moskalenko, Yulia E., Junqueira, Helena C., Baptista, Maurício S., Marques, Carlos M., Machini, M. Terêsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044864/
https://www.ncbi.nlm.nih.gov/pubmed/30023576
http://dx.doi.org/10.1021/acsomega.7b01127
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author Okuda-Shinagawa, Nancy M.
Moskalenko, Yulia E.
Junqueira, Helena C.
Baptista, Maurício S.
Marques, Carlos M.
Machini, M. Terêsa
author_facet Okuda-Shinagawa, Nancy M.
Moskalenko, Yulia E.
Junqueira, Helena C.
Baptista, Maurício S.
Marques, Carlos M.
Machini, M. Terêsa
author_sort Okuda-Shinagawa, Nancy M.
collection PubMed
description [Image: see text] Conjugates based on cell-penetrating peptides (CPPs) are scientifically relevant owing to their structural complexity; their ability to enter cells and deliver drugs, labels, antioxidants, bioactive compounds, or DNA fragments; and, consequently, their potential for application in research and biomedicine. In this study, carboxyamidated fluorescently labeled conjugates FAM-GG-TAT(47-57)-NH(2) and FAM-PEG(6)-TAT(47-57)-NH(2) and photosensitizer-labeled conjugate Ch(k)-PEG(6)-TAT(47-57)-NH(2) [where TAT(47-57) is the CPP, 5(6)-carboxyfluorescein is the (FAM) fluorophore, chlorin k (Ch(k)) is the photosensitizer, and the dipeptide glycyl–glycine (GG) or hexaethylene glycol (PEG(6)) is the spacer] were originally designed, prepared, and fully characterized. Practically, all chemical reactions of the synthetic steps (peptide synthesis, spacer incorporation, and conjugation) were microwave-assisted at 60 °C using optimized protocols to give satisfying yields and high-quality products. Detailed analyses of the conjugates using spectrofluorimetry and singlet oxygen detection showed that they display photophysical properties typical of FAM or Ch(k). Anticandidal activity assays showed that not only this basic property of TAT(47-57) was preserved in the conjugates but also that the minimal inhibitory concentration was slightly reduced for cells incubated with PS-bearing conjugate Ch(k)-PEG(6)-TAT(47-57)-NH(2). Overall, these results indicated that the synthetic approach on-resin assisted by microwaves at 60 °C is simple, straightforward, selective, metal-free, sufficiently fast, cleaner, and more cost-effective than those previously used for preparing this type of macromolecule. Furthermore, such new data show that microwaves at 60 °C and/or conjugation did not harm the integrity of the conjugates’ constituents. Therefore, FAM-GG-TAT(47-57)-NH(2), FAM-PEG(6)-TAT(47-57)-NH(2), and Ch(k)-PEG(6)-TAT(47-57)-NH(2) have high potential for practical applications in biochemistry, biophysics, and therapeutics.
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spelling pubmed-60448642018-07-16 Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties Okuda-Shinagawa, Nancy M. Moskalenko, Yulia E. Junqueira, Helena C. Baptista, Maurício S. Marques, Carlos M. Machini, M. Terêsa ACS Omega [Image: see text] Conjugates based on cell-penetrating peptides (CPPs) are scientifically relevant owing to their structural complexity; their ability to enter cells and deliver drugs, labels, antioxidants, bioactive compounds, or DNA fragments; and, consequently, their potential for application in research and biomedicine. In this study, carboxyamidated fluorescently labeled conjugates FAM-GG-TAT(47-57)-NH(2) and FAM-PEG(6)-TAT(47-57)-NH(2) and photosensitizer-labeled conjugate Ch(k)-PEG(6)-TAT(47-57)-NH(2) [where TAT(47-57) is the CPP, 5(6)-carboxyfluorescein is the (FAM) fluorophore, chlorin k (Ch(k)) is the photosensitizer, and the dipeptide glycyl–glycine (GG) or hexaethylene glycol (PEG(6)) is the spacer] were originally designed, prepared, and fully characterized. Practically, all chemical reactions of the synthetic steps (peptide synthesis, spacer incorporation, and conjugation) were microwave-assisted at 60 °C using optimized protocols to give satisfying yields and high-quality products. Detailed analyses of the conjugates using spectrofluorimetry and singlet oxygen detection showed that they display photophysical properties typical of FAM or Ch(k). Anticandidal activity assays showed that not only this basic property of TAT(47-57) was preserved in the conjugates but also that the minimal inhibitory concentration was slightly reduced for cells incubated with PS-bearing conjugate Ch(k)-PEG(6)-TAT(47-57)-NH(2). Overall, these results indicated that the synthetic approach on-resin assisted by microwaves at 60 °C is simple, straightforward, selective, metal-free, sufficiently fast, cleaner, and more cost-effective than those previously used for preparing this type of macromolecule. Furthermore, such new data show that microwaves at 60 °C and/or conjugation did not harm the integrity of the conjugates’ constituents. Therefore, FAM-GG-TAT(47-57)-NH(2), FAM-PEG(6)-TAT(47-57)-NH(2), and Ch(k)-PEG(6)-TAT(47-57)-NH(2) have high potential for practical applications in biochemistry, biophysics, and therapeutics. American Chemical Society 2017-11-20 /pmc/articles/PMC6044864/ /pubmed/30023576 http://dx.doi.org/10.1021/acsomega.7b01127 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Okuda-Shinagawa, Nancy M.
Moskalenko, Yulia E.
Junqueira, Helena C.
Baptista, Maurício S.
Marques, Carlos M.
Machini, M. Terêsa
Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title_full Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title_fullStr Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title_full_unstemmed Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title_short Fluorescent and Photosensitizing Conjugates of Cell-Penetrating Peptide TAT(47-57): Design, Microwave-Assisted Synthesis at 60 °C, and Properties
title_sort fluorescent and photosensitizing conjugates of cell-penetrating peptide tat(47-57): design, microwave-assisted synthesis at 60 °c, and properties
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044864/
https://www.ncbi.nlm.nih.gov/pubmed/30023576
http://dx.doi.org/10.1021/acsomega.7b01127
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