TY - JOUR
T1 - Protein nanoparticles are nontoxic, tuneable cell stressors
AU - De Pinho Favaro, Marianna Teixeira
AU - Sánchez-García, Laura
AU - Sánchez-Chardi, Alejandro
AU - Roldán, Mónica
AU - Unzueta, Ugutz
AU - Serna, Naroa
AU - Cano-Garrido, Olivia
AU - Azzoni, Adriano Rodrigues
AU - Ferrer-Miralles, Neus
AU - Villaverde, Antonio
AU - Vázquez, Esther
PY - 2018/2/1
Y1 - 2018/2/1
N2 - © 2018 2018 Future Medicine Ltd. Aim: Nanoparticle-cell interactions can promote cell toxicity and stimulate particular behavioral patterns, but cell responses to protein nanomaterials have been poorly studied. Results: By repositioning oligomerization domains in a simple, modular self-assembling protein platform, we have generated closely related but distinguishable homomeric nanoparticles. Composed by building blocks with modular domains arranged in different order, they share amino acid composition. These materials, once exposed to cultured cells, are differentially internalized in absence of toxicity and trigger distinctive cell adaptive responses, monitored by the emission of tubular filopodia and enhanced drug sensitivity. Conclusion: The capability to rapidly modulate such cell responses by conventional protein engineering reveals protein nanoparticles as tuneable, versatile and potent cell stressors for cell-targeted conditioning.
AB - © 2018 2018 Future Medicine Ltd. Aim: Nanoparticle-cell interactions can promote cell toxicity and stimulate particular behavioral patterns, but cell responses to protein nanomaterials have been poorly studied. Results: By repositioning oligomerization domains in a simple, modular self-assembling protein platform, we have generated closely related but distinguishable homomeric nanoparticles. Composed by building blocks with modular domains arranged in different order, they share amino acid composition. These materials, once exposed to cultured cells, are differentially internalized in absence of toxicity and trigger distinctive cell adaptive responses, monitored by the emission of tubular filopodia and enhanced drug sensitivity. Conclusion: The capability to rapidly modulate such cell responses by conventional protein engineering reveals protein nanoparticles as tuneable, versatile and potent cell stressors for cell-targeted conditioning.
KW - molecular therapy
KW - nanoparticles
KW - recombinant proteins
KW - self-assembling
KW - stressor
U2 - https://doi.org/10.2217/nnm-2017-0294
DO - https://doi.org/10.2217/nnm-2017-0294
M3 - Article
SN - 1743-5889
VL - 13
SP - 255
EP - 268
JO - Nanomedicine
JF - Nanomedicine
IS - 3
ER -