Real-time amyloid aggregation monitoring with a photonic crystal-based approach.


We propose the application of a new label-free optical technique based on photonic nanostructures to real-time monitor the amyloid-beta 1-42 (Aβ(1-42)) fibrillization, including the early stages of the aggregation process, which are related to the onset of the Alzheimer's Disease (AD). The aggregation of Aβ peptides into amyloid fibrils has commonly been associated with neuronal death, which culminates in the clinical features of the incurable degenerative AD. Recent studies revealed that cell toxicity is determined by the formation of soluble oligomeric forms of Aβ peptides in the early stages of aggregation. At this phase, classical amyloid detection techniques lack in sensitivity. Upon a chemical passivation of the sensing surface by means of polyethylene glycol, the proposed approach allows an accurate, real-time monitoring of the refractive index variation of the solution, wherein Aβ(1-42) peptides are aggregating. This measurement is directly related to the aggregation state of the peptide throughout oligomerization and subsequent fibrillization. Our findings open new perspectives in the understanding of the dynamics of amyloid formation, and validate this approach as a new and powerful method to screen aggregation at early stages.

DOI: 10.1002/cphc.201300633

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@article{Santi2013RealtimeAA, title={Real-time amyloid aggregation monitoring with a photonic crystal-based approach.}, author={Sara Santi and Valeria Musi and Emiliano Descrovi and Vincent Paeder and Joab Di Francesco and Lubos Hvozdara and Peter Dow van der Wal and Hilal A Lashuel and Annalisa Pastore and Reinhard Neier and Hans Peter Herzig}, journal={Chemphyschem : a European journal of chemical physics and physical chemistry}, year={2013}, volume={14 15}, pages={3476-82} }