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Protein-Engineered Fibers For Drug Encapsulation Traceable via (19)F Magnetic Resonance
[Image: see text] Theranostic materials research is experiencing rapid growth driven by the interest in integrating both therapeutic and diagnostic modalities. These materials offer the unique capability to not only provide treatment but also track the progression of a disease. However, to create an...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682962/ https://www.ncbi.nlm.nih.gov/pubmed/38037605 http://dx.doi.org/10.1021/acsanm.3c04357 |
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author | Britton, Dustin Legocki, Jakub Aristizabal, Orlando Mishkit, Orin Liu, Chengliang Jia, Sihan Renfrew, Paul Douglas Bonneau, Richard Wadghiri, Youssef Z. Montclare, Jin Kim |
author_facet | Britton, Dustin Legocki, Jakub Aristizabal, Orlando Mishkit, Orin Liu, Chengliang Jia, Sihan Renfrew, Paul Douglas Bonneau, Richard Wadghiri, Youssef Z. Montclare, Jin Kim |
author_sort | Britton, Dustin |
collection | PubMed |
description | [Image: see text] Theranostic materials research is experiencing rapid growth driven by the interest in integrating both therapeutic and diagnostic modalities. These materials offer the unique capability to not only provide treatment but also track the progression of a disease. However, to create an ideal theranostic biomaterial without compromising drug encapsulation, diagnostic imaging must be optimized for improved sensitivity and spatial localization. Herein, we create a protein-engineered fluorinated coiled-coil fiber, Q2(TFL), capable of improved sensitivity to (19)F magnetic resonance spectroscopy (MRS) detection. Leveraging residue-specific noncanonical amino acid incorporation of trifluoroleucine (TFL) into the coiled-coil, Q2, which self-assembles into nanofibers, we generate Q2(TFL). We demonstrate that fluorination results in a greater increase in thermostability and (19)F magnetic resonance detection compared to the nonfluorinated parent, Q2. Q2(TFL) also exhibits linear ratiometric (19)F MRS thermoresponsiveness, allowing it to act as a temperature probe. Furthermore, we explore the ability of Q2(TFL) to encapsulate the anti-inflammatory small molecule, curcumin (CCM), and its impact on the coiled-coil structure. Q2(TFL) also provides hyposignal contrast in (1)H MRI, echogenic signal with high-frequency ultrasound and sensitive detection by (19)F MRS in vivo illustrating fluorination of coiled-coils for supramolecular assembly and their use with (1)H MRI, (19)F MRS and high frequency ultrasound as multimodal theranostic agents. |
format | Online Article Text |
id | pubmed-10682962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106829622023-11-30 Protein-Engineered Fibers For Drug Encapsulation Traceable via (19)F Magnetic Resonance Britton, Dustin Legocki, Jakub Aristizabal, Orlando Mishkit, Orin Liu, Chengliang Jia, Sihan Renfrew, Paul Douglas Bonneau, Richard Wadghiri, Youssef Z. Montclare, Jin Kim ACS Appl Nano Mater [Image: see text] Theranostic materials research is experiencing rapid growth driven by the interest in integrating both therapeutic and diagnostic modalities. These materials offer the unique capability to not only provide treatment but also track the progression of a disease. However, to create an ideal theranostic biomaterial without compromising drug encapsulation, diagnostic imaging must be optimized for improved sensitivity and spatial localization. Herein, we create a protein-engineered fluorinated coiled-coil fiber, Q2(TFL), capable of improved sensitivity to (19)F magnetic resonance spectroscopy (MRS) detection. Leveraging residue-specific noncanonical amino acid incorporation of trifluoroleucine (TFL) into the coiled-coil, Q2, which self-assembles into nanofibers, we generate Q2(TFL). We demonstrate that fluorination results in a greater increase in thermostability and (19)F magnetic resonance detection compared to the nonfluorinated parent, Q2. Q2(TFL) also exhibits linear ratiometric (19)F MRS thermoresponsiveness, allowing it to act as a temperature probe. Furthermore, we explore the ability of Q2(TFL) to encapsulate the anti-inflammatory small molecule, curcumin (CCM), and its impact on the coiled-coil structure. Q2(TFL) also provides hyposignal contrast in (1)H MRI, echogenic signal with high-frequency ultrasound and sensitive detection by (19)F MRS in vivo illustrating fluorination of coiled-coils for supramolecular assembly and their use with (1)H MRI, (19)F MRS and high frequency ultrasound as multimodal theranostic agents. American Chemical Society 2023-11-06 /pmc/articles/PMC10682962/ /pubmed/38037605 http://dx.doi.org/10.1021/acsanm.3c04357 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Britton, Dustin Legocki, Jakub Aristizabal, Orlando Mishkit, Orin Liu, Chengliang Jia, Sihan Renfrew, Paul Douglas Bonneau, Richard Wadghiri, Youssef Z. Montclare, Jin Kim Protein-Engineered Fibers For Drug Encapsulation Traceable via (19)F Magnetic Resonance |
title | Protein-Engineered Fibers For Drug Encapsulation Traceable
via (19)F Magnetic Resonance |
title_full | Protein-Engineered Fibers For Drug Encapsulation Traceable
via (19)F Magnetic Resonance |
title_fullStr | Protein-Engineered Fibers For Drug Encapsulation Traceable
via (19)F Magnetic Resonance |
title_full_unstemmed | Protein-Engineered Fibers For Drug Encapsulation Traceable
via (19)F Magnetic Resonance |
title_short | Protein-Engineered Fibers For Drug Encapsulation Traceable
via (19)F Magnetic Resonance |
title_sort | protein-engineered fibers for drug encapsulation traceable
via (19)f magnetic resonance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682962/ https://www.ncbi.nlm.nih.gov/pubmed/38037605 http://dx.doi.org/10.1021/acsanm.3c04357 |
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