MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, PR China.
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, College of Chemistry, Nankai University, Tianjin 300071, PR China.
Anal Chem. 2022 Nov 15;94(45):15902-15907. doi: 10.1021/acs.analchem.2c04042. Epub 2022 Nov 3.
The photooxygenation of amyloid-β (Aβ) protein is considered a promising strategy against Alzheimer's disease (AD). The inhibition of Aβ aggregation or depolymerization of Aβ aggregates can effectively alleviate and improve the condition of AD. Herein, we report a series of "off-on" near-infrared quinolinium photosensitizers (QM20-QM22) based on D-π-A structures using a target-sensing catalyst activation (TaSCAc) strategy. They exhibit turn-on fluorescence when bonded to Aβ aggregates and generate singlet oxygen to achieve the specific imaging and photooxygenation of Aβ aggregates, leading to attenuated Aβ aggregates, enhancing their clearance through the microglial lysosomal pathway, decreasing their neurotoxicity. This study will shed light on the development of the photooxygenation of misfolded proteins for the treatment of neurodegenerative diseases.
淀粉样蛋白(Aβ)的光氧化被认为是对抗阿尔茨海默病(AD)的一种有前途的策略。抑制 Aβ聚集或 Aβ聚集物的解聚可以有效缓解和改善 AD 病情。在此,我们报告了一系列基于 D-π-A 结构的“开-关”近红外喹啉𬭩光增敏剂(QM20-QM22),使用了靶传感催化剂激活(TaSCAc)策略。当它们与 Aβ聚集物结合时,会发出开启的荧光,并产生单线态氧,从而实现 Aβ聚集物的特异性成像和光氧化,导致 Aβ聚集物减少,通过小胶质细胞溶酶体途径增强其清除,降低其神经毒性。本研究将为治疗神经退行性疾病的错误折叠蛋白的光氧化治疗提供新的思路。