Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains

Abstract Materials that respond to temporally defined exogenous cues continue to be an active pursuit of research toward on‐demand nanoparticle drug delivery applications, and using one or more exogenous temperature stimuli could significantly expand the application of nanoparticle‐based drug delive...

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Main Authors: Lucas C. Dunshee, Millicent O. Sullivan, Kristi L. Kiick
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Bioengineering & Translational Medicine
Online Access:https://doi.org/10.1002/btm2.10145
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spelling doaj-fe8c5fa22be2444abb6d7dc558bdf2492020-11-25T01:44:27ZengWileyBioengineering & Translational Medicine2380-67612020-01-0151n/an/a10.1002/btm2.10145Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domainsLucas C. Dunshee0Millicent O. Sullivan1Kristi L. Kiick2Department of Chemical and Biomolecular Engineering University of Delaware Newark DelawareDepartment of Chemical and Biomolecular Engineering University of Delaware Newark DelawareDepartment of Materials Science and Engineering University of Delaware Newark DelawareAbstract Materials that respond to temporally defined exogenous cues continue to be an active pursuit of research toward on‐demand nanoparticle drug delivery applications, and using one or more exogenous temperature stimuli could significantly expand the application of nanoparticle‐based drug delivery formulations under both hyperthermal and hypothermal conditions. Previously we have reported the development of a biocompatible and thermoresponsive elastin‐b‐collagen‐like polypeptide (ELP‐CLP) conjugate that is capable of self‐assembling into vesicles and encapsulating small molecule therapeutics that can be delivered at different rates via a single temperature stimulus. Herein we report the evaluation of multiple ELP‐CLP conjugates, demonstrating that the inverse transition temperature (Tt) of the ELP‐CLPs can be manipulated by modifying the melting temperature (Tm) of the CLP domain, and that the overall hydrophilicity of the ELP‐CLP conjugate also may alter the Tt. Based on these design parameters, we demonstrate that the ELP‐CLP sequence (VPGFG)6‐(GPO)7GG can self‐assemble into stable vesicles at 25°C and dissociate at elevated temperatures by means of the unfolding of the CLP domain above its Tm. We also demonstrate here for the first time the ability of this ELP‐CLP vesicle to dissociate via a hypothermic temperature stimulus by means of exploiting the inverse transition temperature (Tt) phenomena found in ELPs. The development of design rules for manipulating the thermal properties of these bioconjugates will enable future modifications to either the ELP or CLP sequences to more finely tune the transitions of the conjugates for specific biomedical applications.https://doi.org/10.1002/btm2.10145
collection DOAJ
language English
format Article
sources DOAJ
author Lucas C. Dunshee
Millicent O. Sullivan
Kristi L. Kiick
spellingShingle Lucas C. Dunshee
Millicent O. Sullivan
Kristi L. Kiick
Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
Bioengineering & Translational Medicine
author_facet Lucas C. Dunshee
Millicent O. Sullivan
Kristi L. Kiick
author_sort Lucas C. Dunshee
title Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
title_short Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
title_full Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
title_fullStr Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
title_full_unstemmed Manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
title_sort manipulation of the dually thermoresponsive behavior of peptide‐based vesicles through modification of collagen‐like peptide domains
publisher Wiley
series Bioengineering & Translational Medicine
issn 2380-6761
publishDate 2020-01-01
description Abstract Materials that respond to temporally defined exogenous cues continue to be an active pursuit of research toward on‐demand nanoparticle drug delivery applications, and using one or more exogenous temperature stimuli could significantly expand the application of nanoparticle‐based drug delivery formulations under both hyperthermal and hypothermal conditions. Previously we have reported the development of a biocompatible and thermoresponsive elastin‐b‐collagen‐like polypeptide (ELP‐CLP) conjugate that is capable of self‐assembling into vesicles and encapsulating small molecule therapeutics that can be delivered at different rates via a single temperature stimulus. Herein we report the evaluation of multiple ELP‐CLP conjugates, demonstrating that the inverse transition temperature (Tt) of the ELP‐CLPs can be manipulated by modifying the melting temperature (Tm) of the CLP domain, and that the overall hydrophilicity of the ELP‐CLP conjugate also may alter the Tt. Based on these design parameters, we demonstrate that the ELP‐CLP sequence (VPGFG)6‐(GPO)7GG can self‐assemble into stable vesicles at 25°C and dissociate at elevated temperatures by means of the unfolding of the CLP domain above its Tm. We also demonstrate here for the first time the ability of this ELP‐CLP vesicle to dissociate via a hypothermic temperature stimulus by means of exploiting the inverse transition temperature (Tt) phenomena found in ELPs. The development of design rules for manipulating the thermal properties of these bioconjugates will enable future modifications to either the ELP or CLP sequences to more finely tune the transitions of the conjugates for specific biomedical applications.
url https://doi.org/10.1002/btm2.10145
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