Magnetically steerable Fe3O4@Ni2+-NTA-polystyrene nanoparticles for the immobilization and separation of his6-protein

[Display omitted] •Ni2+-NTA-PS NPs encapsulated with magnetic Fe3O4 NPs were synthesized.•The morphology, size and encapsulation were confirmed using SEM, TEM and DLS.•The application of our system was proved by magnetic separation of his6-tag protein. We developed Ni2+-nitrilotriacetic acid (NTA) f...

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Veröffentlicht in:European polymer journal 2019-03, Vol.112, p.524-529
Hauptverfasser: Jose, Leeja, Lee, Chaeyeon, Hwang, Aran, Park, Ji Hyun, Song, Jae Kwang, Paik, Hyun-jong
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container_title European polymer journal
container_volume 112
creator Jose, Leeja
Lee, Chaeyeon
Hwang, Aran
Park, Ji Hyun
Song, Jae Kwang
Paik, Hyun-jong
description [Display omitted] •Ni2+-NTA-PS NPs encapsulated with magnetic Fe3O4 NPs were synthesized.•The morphology, size and encapsulation were confirmed using SEM, TEM and DLS.•The application of our system was proved by magnetic separation of his6-tag protein. We developed Ni2+-nitrilotriacetic acid (NTA) functionalized polystyrene (Ni2+-NTA-PS) nanoparticles encapsulated with magnetic Fe3O4 nanoparticles (Fe3O4@Ni2+-NTA-PS nanoparticles) via miniemulsion/solvent evaporation method for the affinity purification of his6-tag recombinant proteins. Fe3O4@Ni2+-NTA-PS nanoparticles have a high surface to volume ratio, which enhanced the protein immobilization efficiency through the specific interaction between his6-tag of protein and Ni2+-NTA end of the polymer. The potential of Fe3O4@Ni2+-NTA-PS nanoparticles is demonstrated by a direct comparison with commercially available Ni2+-NTA-magnetic beads in his6-protein immobilization and recovery. Furthermore, the practical application of Fe3O4@Ni2+-NTA-PS magnetic nanoparticles is illustrated in his6-protein separation from crude cell lysate.
doi_str_mv 10.1016/j.eurpolymj.2019.01.024
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We developed Ni2+-nitrilotriacetic acid (NTA) functionalized polystyrene (Ni2+-NTA-PS) nanoparticles encapsulated with magnetic Fe3O4 nanoparticles (Fe3O4@Ni2+-NTA-PS nanoparticles) via miniemulsion/solvent evaporation method for the affinity purification of his6-tag recombinant proteins. Fe3O4@Ni2+-NTA-PS nanoparticles have a high surface to volume ratio, which enhanced the protein immobilization efficiency through the specific interaction between his6-tag of protein and Ni2+-NTA end of the polymer. The potential of Fe3O4@Ni2+-NTA-PS nanoparticles is demonstrated by a direct comparison with commercially available Ni2+-NTA-magnetic beads in his6-protein immobilization and recovery. Furthermore, the practical application of Fe3O4@Ni2+-NTA-PS magnetic nanoparticles is illustrated in his6-protein separation from crude cell lysate.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.eurpolymj.2019.01.024</doi><tpages>6</tpages></addata></record>
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subjects Beads
Cell lysate purification
Fe3O4 encapsulation
Functionalized polystyrene
His6-protein
Immobilization
Iron oxides
Luminescence
Magnetic fields
Miniemulsion
Nanoparticles
Ni2+-NTA
Nitrilotriacetic acid
Polystyrene
Polystyrene resins
Proteins
Separation
title Magnetically steerable Fe3O4@Ni2+-NTA-polystyrene nanoparticles for the immobilization and separation of his6-protein
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