Abstract

Here, we studied the effect of the size, shape, and surface charge of Au nanoparticles (AuNPs) on amyloid beta (Aβ) aggregation on a total brain lipid-based supported lipid bilayer (brain SLB), a fluid platform that facilitates Aβ-AuNP aggregation process. We found that larger AuNPs induce large and amorphous aggregates on the brain SLB, whereas smaller AuNPs induce protofibrillar Aβ structures. Positively charged AuNPs were more strongly attracted to Aβ than negatively charged AuNPs, and the stronger interactions between AuNPs and Aβ resulted in fewer β-sheets and more random coil structures. We also compared spherical AuNPs, gold nanorods (AuNRs), and gold nanocubes (AuNCs) to study the effect of nanoparticle shape on Aβ aggregation on the brain SLB. Aβ was preferentially bound to the long axis of AuNRs and fewer fibrils were formed whereas all the facets of AuNCs interacted with Aβ to produce the fibril networks. Finally, it was revealed that different nanostructures induce different cytotoxicity on neuroblastoma cells, and, overall, smaller Aβ aggregates induce higher cytotoxicity. The results offer insight into the roles of NPs and brain SLB in Aβ aggregation on the cell membrane and can facilitate the understanding of Aβ-nanostructure co-aggregation mechanism and tuning Aβ aggregate structures.

Highlights

  • We studied the effect of changes in nanoparticle size, shape, and surface charge on Aβ aggregation on a brain supported lipid bilayer (SLB), using Au nanoparticles (AuNPs) with the identical total surface area to exclude the effect of particle surface area (Fig. 1)

  • The dark-field microscopy, Raman spectroscopy, circular dichroism spectroscopy (CD), and transmission electron microscopy (TEM) data were used as analytical tools in this study

  • We studied how Aβ secondary structures affected after incubation with AuNPs on the brain SLB using Surface-enhanced Raman scattering (SERS) and CD spectra (Fig. 3)

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Summary

Introduction

After 6 hr of incubation of Aβ with 20-nm, 50-nm, or 80-nm AuNPs, they mainly formed protofibrils and short fibrils on the brain SLB; under dark-field microscopy, the color of the Aβ aggregates varied with particle size (Fig. 2). The TEM image showed formation of fibrils with densely packed amine-AuNPs, shown by orange coloring in the correlated dark-field image (Fig. 4b).

Results
Conclusion

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