Encapsidated Atom-Transfer Radical Polymerization in Qβ Virus-like Nanoparticles
Author(s) -
Marisa L. Hovlid,
Jolene L. Lau,
Kurt Breitenkamp,
Cody J. Higginson,
Burkhardt Laufer,
Marianne Manchester,
M. G. Finn
Publication year - 2014
Publication title -
acs nano
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/nn502043d
Subject(s) - atom transfer radical polymerization , polymer , polymerization , nanoparticle , capsid , monomer , covalent bond , polymer chemistry , materials science , macromolecule , bioconjugation , radical polymerization , chemical engineering , chemistry , nanotechnology , organic chemistry , biochemistry , engineering , gene
Virus-like particles (VLPs) are unique macromolecular structures that hold great promise in biomedical and biomaterial applications. The interior of the 30 nm-diameter Qβ VLP was functionalized by a three-step process: (1) hydrolytic removal of endogenously packaged RNA, (2) covalent attachment of initiator molecules to unnatural amino acid residues located on the interior capsid surface, and (3) atom-transfer radical polymerization of tertiary amine-bearing methacrylate monomers. The resulting polymer-containing particles were moderately expanded in size; however, biotin-derivatized polymer strands were only very weakly accessible to avidin, suggesting that most of the polymer was confined within the protein shell. The polymer-containing particles were also found to exhibit physical and chemical properties characteristic of positively charged nanostructures, including the ability to easily enter mammalian cells and deliver functional small interfering RNA.
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