Total Internal Reflection Tip-Enhanced Raman Spectroscopy of Tau Fibrils

Total internal reflection tip-enhanced Raman spectroscopy (TIR-TERS) has recently emerged as a promising technique for noninvasive nanoscale chemical characterization of biomolecules. We demonstrate that the TERS enhancement achieved in this experimental configuration is nearly 30 times higher than that in linear polarization and 8 times higher than that in radial polarization using traditional bottom-illumination geometry. TIR-TERS is applied to the study of Tau amyloid fibrils formed with the human full-length Tau protein mixed with heparin. This technique reveals the possibility to perform TERS imaging with 1-4 nm axial and 5-10 nm lateral spatial optical resolution. In these Tau/heparin fibrils, spectral signatures assigned to aromatic amino acid residues (phenylalanine, histidine, and tyrosine) and nonaromatic ones (e.g., cysteine, lysine, arginine, asparagine, and glutamine) are distinctly observed. Amide I and amide III bands can also be detected. In a fibril portion, it is shown that antiparallel beta-sheets and fibril core beta-sheets are abundant and are often localized in amino acid-rich regions where parallel beta-sheets and random coils are present in lower proportions. This first TIR-TERS study on a nonresonant biological sample paves the way for future nanoscale chemical and structural characterization of biomolecules using this performant and original technique.

Automated summary

Total internal reflection tip-enhanced Raman spectroscopy (TIR-TERS) is a promising technique for noninvasive nanoscale chemical characterization of biomolecules. The TERS enhancement achieved in this configuration is significantly higher than that in traditional illumination geometry. TIR-TERS is applied to the study of Tau amyloid fibrils, revealing spectral signatures and structural information of the fibrils.