TY - JOUR
T1 - Engineering multifunctional protein nanoparticles by in vitro disassembling and reassembling of heterologous building blocks
AU - Unzueta, Ugutz
AU - Serna, Naroa
AU - Sánchez-García, Laura
AU - Roldán, Mónica
AU - Sánchez-Chardi, Alejandro
AU - Mangues, Ramón
AU - Villaverde, Antonio
AU - Vázquez, Esther
PY - 2017/11/22
Y1 - 2017/11/22
N2 - © 2017 IOP Publishing Ltd. The engineering of protein self-assembling at the nanoscale allows the generation of functional and biocompatible materials, which can be produced by easy biological fabrication. The combination of cationic and histidine-rich stretches in fusion proteins promotes oligomerization as stable protein-only regular nanoparticles that are composed by a moderate number of building blocks. Among other applications, these materials are highly appealing as tools in targeted drug delivery once empowered with peptidic ligands of cell surface receptors. In this context, we have dissected here this simple technological platform regarding the controlled disassembling and reassembling of the composing building blocks. By applying high salt and imidazole in combination, nanoparticles are disassembled in a process that is fully reversible upon removal of the disrupting agents. By taking this approach, we accomplish here the in vitro generation of hybrid nanoparticles formed by heterologous building blocks. This fact demonstrates the capability to generate multifunctional and/or multiparatopic or multispecific materials usable in nanomedical applications.
AB - © 2017 IOP Publishing Ltd. The engineering of protein self-assembling at the nanoscale allows the generation of functional and biocompatible materials, which can be produced by easy biological fabrication. The combination of cationic and histidine-rich stretches in fusion proteins promotes oligomerization as stable protein-only regular nanoparticles that are composed by a moderate number of building blocks. Among other applications, these materials are highly appealing as tools in targeted drug delivery once empowered with peptidic ligands of cell surface receptors. In this context, we have dissected here this simple technological platform regarding the controlled disassembling and reassembling of the composing building blocks. By applying high salt and imidazole in combination, nanoparticles are disassembled in a process that is fully reversible upon removal of the disrupting agents. By taking this approach, we accomplish here the in vitro generation of hybrid nanoparticles formed by heterologous building blocks. This fact demonstrates the capability to generate multifunctional and/or multiparatopic or multispecific materials usable in nanomedical applications.
KW - cell targeting
KW - multifunctional nanoparticles
KW - recombinant proteins
KW - self-assembling
KW - viral mimetics
U2 - 10.1088/1361-6528/aa963e
DO - 10.1088/1361-6528/aa963e
M3 - Article
SN - 0957-4484
VL - 28
JO - Nanotechnology
JF - Nanotechnology
IS - 50
M1 - 505102
ER -