研究目的
To provide a detailed protocol for using resonance-enhanced atomic force microscopy infrared spectroscopy (AFM-IR) to characterize the structural composition and heterogeneity of individual extracellular vesicles (EVs) at nanoscale resolution, enabling label-free detection of lipids, proteins, and nucleic acids within single EVs.
研究成果
The AFM-IR protocol enables high-resolution, label-free characterization of EV heterogeneity at the nanoscale, revealing differences in molecular composition within and between EV populations. This approach has potential applications in disease diagnosis, EV therapy development, and understanding EV biology, but requires further validation and optimization for broader use.
研究不足
Smaller vesicles (20-50 nm) may not provide strong IR signals, requiring concentrated samples that can lead to aggregation. AFM-IR imaging is semiquantitative due to possible nonlinearities in energy absorption, and biological samples like EVs are inherently heterogeneous. Polarization effects could influence results if samples are oriented, though EVs are not expected to be oriented. The method requires careful optimization and may not be suitable for very small vesicles without signal enhancement.