4.8 Article

Optical Nanosensor for Intracellular and Intracranial Detection of Amyloid-Beta

期刊

ACS NANO
卷 16, 期 5, 页码 7269-7283

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c00054

关键词

biosensor; fluorescence; neurodegenerative disease; nanocarbon; carbon nanomaterials

资金

  1. NCI
  2. Cancer Center Support Grant [P30-CA008748]
  3. NINDS [R01NS116353]
  4. NIA [R01AG061350]
  5. National Science Foundation CAREER Award [1752506]
  6. JPB Foundation [MR-2020-2155]
  7. Ara Parseghian Medical Research Fund
  8. American Cancer Society Research Scholar Grant [GC230452]
  9. Pershing Square Sohn Cancer Research Alliance
  10. Honorable Tina Brozman Foundation for Ovarian Cancer Research
  11. Expect Miracles Foundation-Financial Services Against Cancer
  12. Anna Fuller Fund
  13. Louis and Rachel Rudin Foundation
  14. Emerson Collective
  15. MSK's Cycle for Survival's Equinox Innovation Award in Rare Cancers
  16. Alan and Sandra Gerry Metastasis Research Initiative
  17. Commonwealth Foundation for Cancer Research
  18. Experimental Therapeutics Center of Memorial Sloan Kettering Cancer Center
  19. Joe W. and Dorothy Dorsett Brown Foundation
  20. PhRMA Foundation Predoctoral Fellowship
  21. Div Of Chem, Bioeng, Env, & Transp Sys
  22. Directorate For Engineering [1752506] Funding Source: National Science Foundation

向作者/读者索取更多资源

The researchers developed a near-infrared optical nanosensor that can detect the presence of A beta in live cells and mice. The sensor selectively responds to A beta through solvatochromic modulation, allowing for tracking of A beta accumulation. This technology provides insight into the molecular mechanisms underlying A beta neurotoxicity in the development of Alzheimer's disease.
Amyloid-beta (A beta) deposition occurs in the early stages of Alzheimer's disease (AD), but the early detection of A beta is a persistent challenge. Herein, we engineered a near-infrared optical nanosensor capable of detecting A beta intracellularly in live cells and intracranially in vivo. The sensor is composed of single-walled carbon nanotubes functionalized with A beta wherein A beta-A beta interactions drive the response. We found that the A beta nanosensors selectively responded to A beta via solvatochromic modulation of the near-infrared emission of the nanotube. The sensor tracked A beta accumulation in live cells and, upon intracranial administration in a genetic model of AD, signaled distinct responses in aged mice. This technology enables the interrogation of molecular mechanisms underlying A beta neurotoxicity in the development of AD in living systems.

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