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Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene

BACKGROUND: Graphene is the 2D form of carbon that exists as a single layer of atoms arranged in a honeycomb lattice and has attracted great interest in the last decade in view of its physical, chemical, electrical, elastic, thermal, and biocompatible properties. The objective of this study was to s...

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Autores principales: Gurunathan, Sangiliyandi, Woong Han, Jae, Kim, Eunsu, Kwon, Deug-Nam, Park, Jin-Ki, Kim, Jin-Hoi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193993/
https://www.ncbi.nlm.nih.gov/pubmed/25273520
http://dx.doi.org/10.1186/s12951-014-0041-9
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author Gurunathan, Sangiliyandi
Woong Han, Jae
Kim, Eunsu
Kwon, Deug-Nam
Park, Jin-Ki
Kim, Jin-Hoi
author_facet Gurunathan, Sangiliyandi
Woong Han, Jae
Kim, Eunsu
Kwon, Deug-Nam
Park, Jin-Ki
Kim, Jin-Hoi
author_sort Gurunathan, Sangiliyandi
collection PubMed
description BACKGROUND: Graphene is the 2D form of carbon that exists as a single layer of atoms arranged in a honeycomb lattice and has attracted great interest in the last decade in view of its physical, chemical, electrical, elastic, thermal, and biocompatible properties. The objective of this study was to synthesize an environmentally friendly and simple methodology for the preparation of graphene using a recombinant enhanced green fluorescent protein (EGFP). RESULTS: The successful reduction of GO to graphene was confirmed using UV–vis spectroscopy, and FT-IR. DLS and SEM were employed to demonstrate the particle size and surface morphology of GO and EGFP-rGO. The results from Raman spectroscopy suggest the removal of oxygen-containing functional groups from the surface of GO and formation of graphene with defects. The biocompatibility analysis of GO and EGFP-rGO in human embryonic kidney (HEK) 293 cells suggests that GO induces significant concentration-dependent cell toxicity in HEK cells, whereas graphene exerts no adverse effects on HEK cells even at a higher concentration (100 μg/mL). CONCLUSIONS: Altogether, our findings suggest that recombinant EGFP can be used as a reducing and stabilizing agent for the preparation of biocompatible graphene. The novelty and originality of this work is that it describes a safe, simple, and environmentally friendly method for the production of graphene using recombinant enhanced green fluorescent protein. Furthermore, the synthesized graphene shows excellent biocompatibility with HEK cells; therefore, biologically synthesized graphene can be used for biomedical applications. To the best of our knowledge, this is the first and novel report describing the synthesis of graphene using recombinant EGFP.
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spelling pubmed-41939932014-10-12 Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene Gurunathan, Sangiliyandi Woong Han, Jae Kim, Eunsu Kwon, Deug-Nam Park, Jin-Ki Kim, Jin-Hoi J Nanobiotechnology Research BACKGROUND: Graphene is the 2D form of carbon that exists as a single layer of atoms arranged in a honeycomb lattice and has attracted great interest in the last decade in view of its physical, chemical, electrical, elastic, thermal, and biocompatible properties. The objective of this study was to synthesize an environmentally friendly and simple methodology for the preparation of graphene using a recombinant enhanced green fluorescent protein (EGFP). RESULTS: The successful reduction of GO to graphene was confirmed using UV–vis spectroscopy, and FT-IR. DLS and SEM were employed to demonstrate the particle size and surface morphology of GO and EGFP-rGO. The results from Raman spectroscopy suggest the removal of oxygen-containing functional groups from the surface of GO and formation of graphene with defects. The biocompatibility analysis of GO and EGFP-rGO in human embryonic kidney (HEK) 293 cells suggests that GO induces significant concentration-dependent cell toxicity in HEK cells, whereas graphene exerts no adverse effects on HEK cells even at a higher concentration (100 μg/mL). CONCLUSIONS: Altogether, our findings suggest that recombinant EGFP can be used as a reducing and stabilizing agent for the preparation of biocompatible graphene. The novelty and originality of this work is that it describes a safe, simple, and environmentally friendly method for the production of graphene using recombinant enhanced green fluorescent protein. Furthermore, the synthesized graphene shows excellent biocompatibility with HEK cells; therefore, biologically synthesized graphene can be used for biomedical applications. To the best of our knowledge, this is the first and novel report describing the synthesis of graphene using recombinant EGFP. BioMed Central 2014-10-03 /pmc/articles/PMC4193993/ /pubmed/25273520 http://dx.doi.org/10.1186/s12951-014-0041-9 Text en © Gurunathan et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gurunathan, Sangiliyandi
Woong Han, Jae
Kim, Eunsu
Kwon, Deug-Nam
Park, Jin-Ki
Kim, Jin-Hoi
Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title_full Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title_fullStr Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title_full_unstemmed Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title_short Enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
title_sort enhanced green fluorescent protein-mediated synthesis of biocompatible graphene
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193993/
https://www.ncbi.nlm.nih.gov/pubmed/25273520
http://dx.doi.org/10.1186/s12951-014-0041-9
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