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Synthesis of protein conjugates adsorbed on cationic liposomes surface

The well-known Toll like receptor 9 (TLR9) agonist CpG ODN has shown promising results as vaccine adjuvant in preclinical and clinical studies, however its in vivo • The CpG ODN Toll-like receptor (TLR) 9 agonist was conjugated to protein antigens via thiol-maleimide chemistry. • Due to their negati...

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Autores principales: Chatzikleanthous, Despo, Cunliffe, Robert, Carboni, Filippo, Romano, Maria Rosaria, O'Hagan, Derek T., Roberts, Craig W., Perrie, Yvonne, Adamo, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289768/
https://www.ncbi.nlm.nih.gov/pubmed/32551244
http://dx.doi.org/10.1016/j.mex.2020.100942
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author Chatzikleanthous, Despo
Cunliffe, Robert
Carboni, Filippo
Romano, Maria Rosaria
O'Hagan, Derek T.
Roberts, Craig W.
Perrie, Yvonne
Adamo, Roberto
author_facet Chatzikleanthous, Despo
Cunliffe, Robert
Carboni, Filippo
Romano, Maria Rosaria
O'Hagan, Derek T.
Roberts, Craig W.
Perrie, Yvonne
Adamo, Roberto
author_sort Chatzikleanthous, Despo
collection PubMed
description The well-known Toll like receptor 9 (TLR9) agonist CpG ODN has shown promising results as vaccine adjuvant in preclinical and clinical studies, however its in vivo • The CpG ODN Toll-like receptor (TLR) 9 agonist was conjugated to protein antigens via thiol-maleimide chemistry. • Due to their negative charge, protein conjugates readily electrostatically bound cationic liposomes composed of 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), cholesterol and dimethyldioctadecylammonium bromide (DDA) resulting to the design of novel cationic liposomes-protein conjugate complexes. • The method is suited for the liposomal delivery of a variety of adjuvant-protein conjugates.
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spelling pubmed-72897682020-06-17 Synthesis of protein conjugates adsorbed on cationic liposomes surface Chatzikleanthous, Despo Cunliffe, Robert Carboni, Filippo Romano, Maria Rosaria O'Hagan, Derek T. Roberts, Craig W. Perrie, Yvonne Adamo, Roberto MethodsX Pharmacology, Toxicology and Pharmaceutical Science The well-known Toll like receptor 9 (TLR9) agonist CpG ODN has shown promising results as vaccine adjuvant in preclinical and clinical studies, however its in vivo • The CpG ODN Toll-like receptor (TLR) 9 agonist was conjugated to protein antigens via thiol-maleimide chemistry. • Due to their negative charge, protein conjugates readily electrostatically bound cationic liposomes composed of 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), cholesterol and dimethyldioctadecylammonium bromide (DDA) resulting to the design of novel cationic liposomes-protein conjugate complexes. • The method is suited for the liposomal delivery of a variety of adjuvant-protein conjugates. Elsevier 2020-05-28 /pmc/articles/PMC7289768/ /pubmed/32551244 http://dx.doi.org/10.1016/j.mex.2020.100942 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Pharmacology, Toxicology and Pharmaceutical Science
Chatzikleanthous, Despo
Cunliffe, Robert
Carboni, Filippo
Romano, Maria Rosaria
O'Hagan, Derek T.
Roberts, Craig W.
Perrie, Yvonne
Adamo, Roberto
Synthesis of protein conjugates adsorbed on cationic liposomes surface
title Synthesis of protein conjugates adsorbed on cationic liposomes surface
title_full Synthesis of protein conjugates adsorbed on cationic liposomes surface
title_fullStr Synthesis of protein conjugates adsorbed on cationic liposomes surface
title_full_unstemmed Synthesis of protein conjugates adsorbed on cationic liposomes surface
title_short Synthesis of protein conjugates adsorbed on cationic liposomes surface
title_sort synthesis of protein conjugates adsorbed on cationic liposomes surface
topic Pharmacology, Toxicology and Pharmaceutical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289768/
https://www.ncbi.nlm.nih.gov/pubmed/32551244
http://dx.doi.org/10.1016/j.mex.2020.100942
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