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Development of albumin macroinitiator for polymers to use in DNA origami coating

BACKGROUND/AIM: DNA nanostructures have many advantages over polymers and lipid based drug delivery agents such as biodegradability and biocompatibility. However their transfection rates and stability still limit their widely use in nanomedicine. In this study highly versatile and straightforward al...

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Autores principales: BİLİR, Aykut, EMÜL, Ezgi, SAĞLAM, Necdet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491299/
https://www.ncbi.nlm.nih.gov/pubmed/32283899
http://dx.doi.org/10.3906/sag-2001-245
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author BİLİR, Aykut
EMÜL, Ezgi
SAĞLAM, Necdet
author_facet BİLİR, Aykut
EMÜL, Ezgi
SAĞLAM, Necdet
author_sort BİLİR, Aykut
collection PubMed
description BACKGROUND/AIM: DNA nanostructures have many advantages over polymers and lipid based drug delivery agents such as biodegradability and biocompatibility. However their transfection rates and stability still limit their widely use in nanomedicine. In this study highly versatile and straightforward albumin coating preparation method is showed for DNA nanostructures. MATERIALS AND METHODS: N-methylolmaleimide was esterified with a-bromoisobutyrl bromide (BiBB) to achive bromine functional structure. Then it was attached to bovine serum albumin (BSA) via cysteine-maleimide bond further to use as macroinitiator for atom transfer radical polymerization (ATRP). Cationic polymers can be synthesized from this end further to use as binding domain for fabricated 60 Helix bundle DNA origami. RESULTS: Proton nuclear magnetic resonance (1H NMR) analysis used for characterization. Methyelene group hydrogens’ peak in 5.0 ppm and strong peak in 1.5–2.0 ppm range showed proper methylolation of maleimide and bromine functional formation, respectively. Then BSA-macroinitiator formation is verified by 1780 Da peak shift in MALDI-TOF (Matrix-assisted laser desorption/ionization - time of flight) spectrum. Moreover electrophoretic mobility shift assay (EMSA) showed successful dense 60 Helix bundle formation. CONCLUSION: In this study, a facile method is developed to synthesize protein conjugated-ATRP initiator further can be used in polymerization and coating DNA nanostructures. It is feasible for any protein containing cysteine amino acid.
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spelling pubmed-74912992020-09-16 Development of albumin macroinitiator for polymers to use in DNA origami coating BİLİR, Aykut EMÜL, Ezgi SAĞLAM, Necdet Turk J Med Sci Article BACKGROUND/AIM: DNA nanostructures have many advantages over polymers and lipid based drug delivery agents such as biodegradability and biocompatibility. However their transfection rates and stability still limit their widely use in nanomedicine. In this study highly versatile and straightforward albumin coating preparation method is showed for DNA nanostructures. MATERIALS AND METHODS: N-methylolmaleimide was esterified with a-bromoisobutyrl bromide (BiBB) to achive bromine functional structure. Then it was attached to bovine serum albumin (BSA) via cysteine-maleimide bond further to use as macroinitiator for atom transfer radical polymerization (ATRP). Cationic polymers can be synthesized from this end further to use as binding domain for fabricated 60 Helix bundle DNA origami. RESULTS: Proton nuclear magnetic resonance (1H NMR) analysis used for characterization. Methyelene group hydrogens’ peak in 5.0 ppm and strong peak in 1.5–2.0 ppm range showed proper methylolation of maleimide and bromine functional formation, respectively. Then BSA-macroinitiator formation is verified by 1780 Da peak shift in MALDI-TOF (Matrix-assisted laser desorption/ionization - time of flight) spectrum. Moreover electrophoretic mobility shift assay (EMSA) showed successful dense 60 Helix bundle formation. CONCLUSION: In this study, a facile method is developed to synthesize protein conjugated-ATRP initiator further can be used in polymerization and coating DNA nanostructures. It is feasible for any protein containing cysteine amino acid. The Scientific and Technological Research Council of Turkey 2020-08-26 /pmc/articles/PMC7491299/ /pubmed/32283899 http://dx.doi.org/10.3906/sag-2001-245 Text en Copyright © 2020 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
BİLİR, Aykut
EMÜL, Ezgi
SAĞLAM, Necdet
Development of albumin macroinitiator for polymers to use in DNA origami coating
title Development of albumin macroinitiator for polymers to use in DNA origami coating
title_full Development of albumin macroinitiator for polymers to use in DNA origami coating
title_fullStr Development of albumin macroinitiator for polymers to use in DNA origami coating
title_full_unstemmed Development of albumin macroinitiator for polymers to use in DNA origami coating
title_short Development of albumin macroinitiator for polymers to use in DNA origami coating
title_sort development of albumin macroinitiator for polymers to use in dna origami coating
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491299/
https://www.ncbi.nlm.nih.gov/pubmed/32283899
http://dx.doi.org/10.3906/sag-2001-245
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