AI Article Synopsis

  • The study explores how iron oxide-based magnetic nanoparticles (MNPs) interact with cells through protein secretion and employs machine learning-assisted SERS for analysis.
  • The researchers developed various MNPs with different surface modifications, significantly impacting their size, shape, and charge, which were assessed using techniques like transmission electron microscopy (TEM).
  • Results showed that smaller MNPs adhered better to cells, and those encapsulated with polyethylenimine (PEI) enhanced the secretion of the recombinant azurin protein, highlighting the important role of MNP properties in cell interactions and potential applications in protein delivery.

Article Abstract

This study introduces a novel investigation of the interaction between cells and iron oxide-based magnetic nanoparticles (FeO MNPs) via protein secretion and machine learning (ML)-assisted surface-enhanced Raman scattering (SERS). For the first time, we produced FeO, FeO@PEG, FeO@PEI, and FeO@PEI MNPs by a one-pot coprecipitation reaction. The addition of polymers to the reaction conditions significantly affected the shape, surface charge, size, and size distribution of the MNPs. The surface modification of MNPs is effectively accomplished using polyethylenimine (PEI), and the ζ-potential values of the MNPs exceed +25 mV under the NHOH control. The homogeneity of MNPs synthesized with NHOH is more pronounced according to transmission electron microscopy (TEM) pictures. All MNPs exhibited excellent immobilization efficiency (>92%) when we used 250 ppm Fe-containing MNP solutions. Smaller MNPs uniformly encapsulated the surface of cells, whereas larger MNPs exhibited irregular accumulation. cells exhibited excellent viability in all MNP solutions at up to 1000 ppm of Fe concentrations. Finally, the highest recombinant azurin protein secretion rate was obtained in FeO@PEI MNP-immobilized cells (about 1.3 times). The ML-assisted SERS analysis revealed that MNP interactions with cells were mediated by proteins such as mannoproteins and membrane transporter proteins as well as N-acetylglucosamine (i.e., chitin). These findings revealed the effect of the size and surface properties of MNPs on the immobilization of cells and the enormous potential of magnetic immobilization for protein secretion.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11672479PMC
http://dx.doi.org/10.1021/acsami.4c18591DOI Listing

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