Hydrophobization of Tobacco Mosaic Virus to Control the Mineralization of Organic Templates.
ZnS
bio/inorganic hybrid materials
hydrophobization
polymer coupling
tobacco mosaic virus
Journal
Nanomaterials (Basel, Switzerland)
ISSN: 2079-4991
Titre abrégé: Nanomaterials (Basel)
Pays: Switzerland
ID NLM: 101610216
Informations de publication
Date de publication:
24 May 2019
24 May 2019
Historique:
received:
24
04
2019
revised:
20
05
2019
accepted:
20
05
2019
entrez:
30
5
2019
pubmed:
30
5
2019
medline:
30
5
2019
Statut:
epublish
Résumé
The robust, anisotropic tobacco mosaic virus (TMV) provides a monodisperse particle size and defined surface chemistry. Owing to these properties, it became an excellent bio-template for the synthesis of diverse nanostructured organic/inorganic functional materials. For selective mineralization of the bio-template, specific functional groups were introduced by means of different genetically encoded amino acids or peptide sequences into the polar virus surface. An alternative approach for TMV surface functionalization is chemical coupling of organic molecules. To achieve mineralization control in this work, we developed a synthetic strategy to manipulate the surface hydrophilicity of the virus through covalent coupling of polymer molecules. Three different types of polymers, namely the perfluorinated (poly(pentafluorostyrene) (PFS)), the thermo-responsive poly(propylene glycol) acrylate (PPGA), and the block-copolymer polyethylene-block-poly(ethylene glycol) were examined. We have demonstrated that covalent attachment of hydrophobic polymer molecules with proper features retains the integrity of the virus structure. In addition, it was found that the degree of the virus hydrophobicity, examined via a ZnS mineralization test, could be tuned by the polymer properties.
Identifiants
pubmed: 31137720
pii: nano9050800
doi: 10.3390/nano9050800
pmc: PMC6567237
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : BI 469/19-3
Organisme : Deutsche Forschungsgemeinschaft
ID : SE 901/1-3
Organisme : Bundesministerium für Bildung und Forschung (BMBF)
ID : 03SF0531C
Organisme : Carl Zeiss Foundation and University of Stuttgart
ID : Projekthaus NanoBioMater
Références
Beilstein J Nanotechnol. 2016 Apr 25;7:613-29
pubmed: 27335751
Adv Mater. 2011 Nov 9;23(42):4918-22
pubmed: 21959928
ACS Nano. 2010 Sep 28;4(9):5366-72
pubmed: 20707328
J Mol Biol. 1999 Jul 2;290(1):9-20
pubmed: 10388554
Adv Virus Res. 2018;102:149-176
pubmed: 30266172
Science. 2004 Jan 9;303(5655):213-7
pubmed: 14716009
Science. 2003 Sep 26;301(5641):1882-4
pubmed: 14512621
Nature. 2006 Mar 16;440(7082):297-302
pubmed: 16541064
Nanoscale. 2013 May 7;5(9):3808-16
pubmed: 23519401
Nat Nanotechnol. 2006 Oct;1(1):72-7
pubmed: 18654145
Biotechnology (N Y). 1995 Jan;13(1):53-7
pubmed: 9634749
Nanoscale. 2016 Dec 1;8(47):19853-19866
pubmed: 27878174
Small. 2016 Sep;12(36):4955-4959
pubmed: 27061916
Chem Soc Rev. 2012 Jun 7;41(11):4356-78
pubmed: 22531991
Virology. 1998 Apr 25;244(1):13-9
pubmed: 9581773
Biomacromolecules. 2013 Aug 12;14(8):2593-600
pubmed: 23763628
Langmuir. 2008 May 20;24(10):5439-44
pubmed: 18435550
Chem Commun (Camb). 2014 Nov 4;50(85):12977-80
pubmed: 25220879
J Am Chem Soc. 2005 Mar 23;127(11):3718-23
pubmed: 15771505
Langmuir. 2010 Nov 16;26(22):17383-8
pubmed: 20964388
Adv Biosyst. 2017 Nov;1(11):e1700106
pubmed: 32646171
Nano Lett. 2007 Dec;7(12):3729-33
pubmed: 18020388
Biomacromolecules. 2012 Feb 13;13(2):422-31
pubmed: 22188342
Adv Drug Deliv Rev. 2019 May;145:96-118
pubmed: 30176280
Biotechnol J. 2018 Dec;13(12):e1800147
pubmed: 30288951
Langmuir. 2004 Jan 20;20(2):441-7
pubmed: 15743089
Adv Mater. 2012 Aug 28;24(33):4557-63
pubmed: 22807140
Phytopathology. 1967 Nov;57(11):1285
pubmed: 6075009
Langmuir. 2015 Apr 7;31(13):3897-903
pubmed: 25768914