4.6 Article

A Label-Free Platform for Identification of Exosomes from Different Sources

期刊

ACS SENSORS
卷 4, 期 2, 页码 488-497

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.8b01564

关键词

exosome; surface-enhanced Raman spectroscopy; graphene; principal component analysis; biomarker

资金

  1. United States Government
  2. American people through the United States Department of State
  3. United States Agency for International Development (USAID) under the Pakistan-U.S Science & Technology Cooperation Program
  4. Zhejiang University Cao Guang-Biao Advanced Science and Technology Fund
  5. Alexander von Humboldt Foundation Research Award
  6. Team Parkinson/Parkinson Alliance
  7. UCLA American Parkinson's Disease Association (APDA) Center
  8. MSA Coalition [2017-10-007]

向作者/读者索取更多资源

Exosomes contain cell- and cell-state-specific cargos of proteins, lipids, and nucleic acids and play significant roles in cell signaling and cell-cell communication. Current research into exosome-based biomarkers has relied largely on analyzing candidate biomarkers, i.e., specific proteins or nucleic acids. However, this approach may miss important biomarkers that are yet to be identified. Alternative approaches are to analyze the entire exosome system, either by omits methods or by techniques that provide fingerprints of the system without identifying each individual biomolecule component. Here, we describe a platform of the latter type, which is based on surface-enhanced Raman spectroscopy (SERS) in combination with multivariate analysis, and demonstrate the utility of this platform for analyzing exosomes derived from different biological sources. First, we examined whether this analysis could use exosomes isolated from fetal bovine serum using a simple, commercially available isolation kit or necessitates the higher purity achieved by the gold standard ultracentrifugation/filtration procedure. Our data demonstrate that the latter method is required for this type of analysis. Having established this requirement, we rigorously analyzed the Raman spectral signature of individual exosomes using a unique, hybrid SERS substrate made of a graphene-covered Au surface containing a quasi-periodic array of pyramids. To examine the source of the Raman signal, we used Raman mapping of low and high spatial resolution combined with morphological identification of exosomes by scanning electron microscopy. Both approaches suggested that the spectra were collected from single exosomes. Finally, we demonstrate for the first time that our platform can distinguish among exosomes from different biological sources based on their Raman signature, a promising approach for developing exosome-based fingerprinting. Our study serves as a solid technological foundation for future exploration of the roles of exosomes in various biological processes and their use as biomarkers for disease diagnosis and treatment monitoring.

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