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用于靶向解离阿尔茨海默病β-淀粉样蛋白聚集体的近红外活性铜铋氧化物电极。

Near-Infrared-Active Copper Bismuth Oxide Electrodes for Targeted Dissociation of Alzheimer's β-Amyloid Aggregates.

机构信息

Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), 335 Science Road, Daejeon 305-701, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 May 27;12(21):23667-23676. doi: 10.1021/acsami.0c02349. Epub 2020 May 14.

Abstract

The abnormal accumulation of β-amyloid (Aβ) aggregates in the brain is a major pathological hallmark of Alzheimer's disease. We report a near-infrared (NIR)-active CuBiO-based photocathodic platform that can target intact Aβ aggregates and dissociate them into nontoxic species. Because of its relatively narrow band gap, CuBiO exhibits strong absorption of NIR light, which allows for deeper tissue penetration and causes less photodamage to tissues compared to visible light. Furthermore, its high stability in aqueous media, biocompatibility, and robustness against photocorrosion make CuBiO an ideal material for medical applications. For the targeted clearance of Aβ aggregates, we have conjugated the KLVFF peptide which specifically recognizes and captures Aβ aggregates on the surface of silver-doped CuBiO (Ag:CuBiO). Upon illumination of NIR light under a cathodic bias, the KLVFF-immobilized Ag:CuBiO (KLVFF-Ag:CuBiO) effectively dissociated β-sheet-rich, long, and entangled Aβ fibrillary aggregates into small fragmented, soluble species through photo-oxygenation. We also verified that the KLVFF-Ag:CuBiO photocathode is biocompatible and effective in reducing Aβ aggregate-induced neurotoxicity. Our work demonstrates the potential of the KLVFF-Ag:CuBiO platform for the targeted disassembly of cytotoxic, robust Aβ aggregates with the aid of NIR energy and cathodic bias.

摘要

β-淀粉样蛋白(Aβ)聚集体在大脑中的异常积累是阿尔茨海默病的主要病理学标志。我们报告了一种近红外(NIR)活性的 CuBiO 基光阴极平台,该平台可以靶向完整的 Aβ聚集体并将其解离成无毒物质。由于其较窄的带隙,CuBiO 对近红外光具有强烈的吸收,与可见光相比,它可以更深地穿透组织并减少对组织的光损伤。此外,其在水介质中的高稳定性、生物相容性和对光腐蚀的鲁棒性使 CuBiO 成为医学应用的理想材料。为了靶向清除 Aβ聚集体,我们已经将专门识别和捕获表面上的 Aβ聚集体的 KLVFF 肽共轭到掺银的 CuBiO(Ag:CuBiO)上。在阴极偏压下照射近红外光时,通过光氧化作用,固定 KLVFF 的 Ag:CuBiO(KLVFF-Ag:CuBiO)有效地将富含β-片层、长且缠结的 Aβ原纤维聚集体解离成小的、可溶性的片段。我们还验证了 KLVFF-Ag:CuBiO 光阴极具有生物相容性,并能有效减轻 Aβ聚集体诱导的神经毒性。我们的工作表明,在近红外能量和阴极偏压的帮助下,KLVFF-Ag:CuBiO 平台具有靶向分解细胞毒性、强韧的 Aβ聚集体的潜力。

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