TY - JOUR
T1 - Biofabrication of functional protein nanoparticles through simple His-tag engineering
AU - López-Laguna, Hèctor
AU - Sánchez, Julieta M.
AU - Carratalá, José Vicente
AU - Rojas-Peña, Mauricio
AU - Sánchez-García, Laura
AU - Parladé, Eloi
AU - Sánchez-Chardi, Alejandro
AU - Voltà-Durán, Eric
AU - Serna, Naroa
AU - Cano-Garrido, Olivia
AU - Flores, Sandra
AU - Ferrer-Miralles, Neus
AU - Nolan, Verónica
AU - De Marco, Ario
AU - Roher, Nerea
AU - Unzueta, Ugutz
AU - Vazquez, Esther
AU - Villaverde, Antonio
N1 - © 2021 American Chemical Society.
PY - 2021/9/13
Y1 - 2021/9/13
N2 - We have developed a simple, robust, and fully transversal approach for the a-la-carte fabrication of functional multimeric nanoparticles with potential biomedical applications, validated here by a set of diverse and unrelated polypeptides. The proposed concept is based on the controlled coordination between Zn2+ ions and His residues in His-tagged proteins. This approach results in a spontaneous and reproducible protein assembly as nanoscale oligomers that keep the original functionalities of the protein building blocks. The assembly of these materials is not linked to particular polypeptide features, and it is based on an environmentally friendly and sustainable approach. The resulting nanoparticles, with dimensions ranging between 10 and 15 nm, are regular in size, are architecturally stable, are fully functional, and serve as intermediates in a more complex assembly process, resulting in the formation of microscale protein materials. Since most of the recombinant proteins produced by biochemical and biotechnological industries and intended for biomedical research are His-tagged, the green biofabrication procedure proposed here can be straightforwardly applied to a huge spectrum of protein species for their conversion into their respective nanostructured formats.
AB - We have developed a simple, robust, and fully transversal approach for the a-la-carte fabrication of functional multimeric nanoparticles with potential biomedical applications, validated here by a set of diverse and unrelated polypeptides. The proposed concept is based on the controlled coordination between Zn2+ ions and His residues in His-tagged proteins. This approach results in a spontaneous and reproducible protein assembly as nanoscale oligomers that keep the original functionalities of the protein building blocks. The assembly of these materials is not linked to particular polypeptide features, and it is based on an environmentally friendly and sustainable approach. The resulting nanoparticles, with dimensions ranging between 10 and 15 nm, are regular in size, are architecturally stable, are fully functional, and serve as intermediates in a more complex assembly process, resulting in the formation of microscale protein materials. Since most of the recombinant proteins produced by biochemical and biotechnological industries and intended for biomedical research are His-tagged, the green biofabrication procedure proposed here can be straightforwardly applied to a huge spectrum of protein species for their conversion into their respective nanostructured formats.
KW - Biomaterials design
KW - Divalent cations
KW - Nanoparticles
KW - Protein engineering
KW - Protein materials
UR - http://www.scopus.com/inward/record.url?scp=85114670247&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/d30fca0d-31e6-33bf-9eac-177548d9a9ed/
U2 - 10.1021/acssuschemeng.1c04256
DO - 10.1021/acssuschemeng.1c04256
M3 - Article
C2 - 34603855
AN - SCOPUS:85114670247
VL - 9
IS - 36
ER -