Photomodulating Carbon Dots for Spatiotemporal Suppression of Alzheimer’s β‑Amyloid Aggregation

Extracellular deposition of β-amyloid (Aβ) peptide aggregates is a major characteristic of Alzheimer’s disease (AD) brain. Because Aβ peptide aggregates aggravate neuropathy and cognitive impairment for AD patients, numerous efforts have been devoted to suppressing Aβ self-assembly as a prospective...

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Veröffentlicht in:ACS nano 2020-12, Vol.14 (12), p.16973-16983
Hauptverfasser: Chung, You Jung, Lee, Chang Heon, Lim, Jinyeong, Jang, Jinhyeong, Kang, Hyuno, Park, Chan Beum
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Sprache:eng
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Zusammenfassung:Extracellular deposition of β-amyloid (Aβ) peptide aggregates is a major characteristic of Alzheimer’s disease (AD) brain. Because Aβ peptide aggregates aggravate neuropathy and cognitive impairment for AD patients, numerous efforts have been devoted to suppressing Aβ self-assembly as a prospective AD treatment option. Here, we report Aβ-targeting, red-light-responsive carbon dots (CDs), and their therapeutic functions as a light-powered nanomodulator to spatiotemporally suppress toxic Aβ aggregation both in vitro and in vivo. Our aptamer-functionalized carbon dots (Apta@CDs) showed strong targeting ability toward Aβ42 species. Moreover, red LED irradiation induced Apta@CDs to irreversibly denature Aβ peptides, impeding the formation of β-sheet-rich Aβ aggregates and attenuating Aβ-associated cytotoxicity. Consequently, Apta@CDs-mediated photomodualtion modality achieved effective suppression of Aβ aggregation in vivo, which significantly reduced the Aβ burden at the targeted sites in the brain of 5xFAD mice by ∼40% and ∼25% according to imaging and ELISA analyses, respectively. Our work demonstrates the therapeutic potential of photomodulating CDs for light-driven suppression against Aβ self-assembly and related neurotoxicity.
ISSN:1936-0851
1936-086X
DOI:10.1021/acsnano.0c06078