Poly(triazolyl methacrylate) glycopolymers as potential targeted unimolecular nanocarriers

UDC.coleccionInvestigaciónes_ES
UDC.departamentoQuímicaes_ES
UDC.endPage21166es_ES
UDC.grupoInvNanochemistry and Self-Assembly for Biological Sciences (NANOSELF4BIO)es_ES
UDC.issue11es_ES
UDC.journalTitleNanoscalees_ES
UDC.startPage21155es_ES
dc.contributor.authorMadeira do O, J.
dc.contributor.authorForalosso, R.
dc.contributor.authorYilmaz, Gokhan
dc.contributor.authorMastrotto, Francesca
dc.contributor.authorKing, P.J.S.
dc.contributor.authorXerri, R. M.
dc.contributor.authorHe, Yinfeng
dc.contributor.authorWalle, Christopher van der
dc.contributor.authorFernández-Trillo, Paco
dc.contributor.authorLaughton, Charles
dc.contributor.authorStyliari, Ioanna Danai
dc.contributor.authorStolnik, Snjezana Snow
dc.contributor.authorMantovani, Giuseppe
dc.date.accessioned2024-07-11T15:45:39Z
dc.date.available2024-07-11T15:45:39Z
dc.date.issued2019
dc.description.abstract[Abstract] Synthetic glycopolymers are increasingly investigated as multivalent ligands for a range of biological and biomedical applications. This study indicates that glycopolymers with a fine-tuned balance between hydrophilic sugar pendant units and relatively hydrophobic polymer backbones can act as single-chain targeted nanocarriers for low molecular weight hydrophobic molecules. Non-covalent complexes formed from poly(triazolyl methacrylate) glycopolymers and low molecular weight hydrophobic guest molecules were characterised through a range of analytical techniques – DLS, SLS, TDA, fluorescence spectroscopy, surface tension analysis – and molecular dynamics (MD) modelling simulations provided further information on the macromolecular characteristics of these single chain complexes. Finally, we show that these nanocarriers can be utilised to deliver a hydrophobic guest molecule, Nile red, to both soluble and surface-immobilised concanavalin A (Con A) and peanut agglutinin (PNA) model lectins with high specificity, showing the potential of non-covalent complexation with specific glycopolymers in targeted guest-molecule delivery.es_ES
dc.description.sponsorshipThis work was supported by the Engineering and Physical Sciences Research Council [grant numbers EP/L01646X, and EP/N024818/1] (RF and RMX, and YH); AstraZeneca (JMdO); and the University of Nottingham. We thank Dr Luisa Martinez-Pomares (University of Nottingham) for supplying MR+ CHO cells, and Dr Annela Seddon (University of Bristol) for useful discussion. All MD simulations were run in GROMACS 5.1.05 using the High Performance Computing (HPC) cluster of the University of Nottingham or ARCHER, UK’s National Supercomputer.es_ES
dc.description.sponsorshipUnited Kindong. Engineering and Physical Sciences Research Council; EP/L01646Xes_ES
dc.description.sponsorshipUnited Kindong. Engineering and Physical Sciences Research Council; EP/L01646Xes_ES
dc.identifier.citationMadeira do O, J., Foralosso, R., Yilmaz, G., Mastrotto, F., King, P.J.S., Xerri, R.M., He, Y., Walle C.F. Van Der, Fernandez-Trillo, F., Laughton, C.A., Styliari, I., Stolnik, S. & Mantovani. G. (2019). Poly(triazolyl methacrylate) glycopolymers as potential targeted unimolecular nanocarriers. Nanoscale, 11(44), 21155-21166. https://doi.org/10.1039/C9NR05836Bes_ES
dc.identifier.doi10.1039/C9NR05836B
dc.identifier.urihttp://hdl.handle.net/2183/37943
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.relation.urihttps://doi.org/10.1039/C9NR05836Bes_ES
dc.rightsCreative Commons Attribution 3.0 Unported Licencees_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectPoly(triazolyl methacrylate) glycopolymerses_ES
dc.subjectTargeted unimolecular nanocarrierses_ES
dc.subjectMethacrylateses_ES
dc.subjectMolecular dynamics simulationses_ES
dc.titlePoly(triazolyl methacrylate) glycopolymers as potential targeted unimolecular nanocarrierses_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication70a74a46-7cea-40e2-85ef-e99554e97bbe
relation.isAuthorOfPublication.latestForDiscovery70a74a46-7cea-40e2-85ef-e99554e97bbe

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