TY - JOUR
T1 - A protein chimera self-assembling unit for drug delivery
AU - Amalfitano, Adriana
AU - Martini, Cecilia
AU - Nocca, Giuseppina
AU - Papi, Massimiliano
AU - De Spirito, Marco
AU - Sanguinetti, Maurizio
AU - Vitali, Alberto
AU - Bugli, Francesca
AU - Arcovito, Alessandro
PY - 2019
Y1 - 2019
N2 - In the modern view of selective drug delivery of bioactive molecules, the attention is moving onto the setup of the perfect carrier more than in the optimization of the active compound. In this respect, virus-like particles constitute bioinspired nanodevices with the intrinsic ability to transport a large class of molecules, ranging from smart drugs to small interfering RNAs. In this work, we demonstrate the efficacy of a novel construct obtained by fusing a self-assembling protein from the human Rotavirus A, VP6, with the Small Ubiquitin Modifier domain, which maintains the ability to form nanoparticles and nanotubes and is able to be used as a drug carrier, even without specific targeting epitopes. The high expression and purification yield, combined with low toxicity of the empty particles, clearly indicate a good candidate for future studies of selective drug delivery. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 2018.
AB - In the modern view of selective drug delivery of bioactive molecules, the attention is moving onto the setup of the perfect carrier more than in the optimization of the active compound. In this respect, virus-like particles constitute bioinspired nanodevices with the intrinsic ability to transport a large class of molecules, ranging from smart drugs to small interfering RNAs. In this work, we demonstrate the efficacy of a novel construct obtained by fusing a self-assembling protein from the human Rotavirus A, VP6, with the Small Ubiquitin Modifier domain, which maintains the ability to form nanoparticles and nanotubes and is able to be used as a drug carrier, even without specific targeting epitopes. The high expression and purification yield, combined with low toxicity of the empty particles, clearly indicate a good candidate for future studies of selective drug delivery. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 2018.
KW - Biotechnology
KW - innovative biotechnologies
KW - personalized medicine
KW - targeted therapy
KW - virus-like particles
KW - Biotechnology
KW - innovative biotechnologies
KW - personalized medicine
KW - targeted therapy
KW - virus-like particles
UR - http://hdl.handle.net/10807/129550
UR - http://onlinelibrary.wiley.com/journal/10.1021/(issn)1520-6033
U2 - 10.1002/btpr.2769
DO - 10.1002/btpr.2769
M3 - Article
SN - 8756-7938
VL - 35
SP - N/A-N/A
JO - Biotechnology Progress
JF - Biotechnology Progress
ER -