Division of Chemistry, Department of Physics, Chemistry and Biology, Linköping University, 581 83, Linköping, Sweden.
Chemistry. 2020 Jun 10;26(33):7425-7432. doi: 10.1002/chem.201905612. Epub 2020 May 15.
Protein deposits are associated with many devastating diseases and fluorescent ligands able to visualize these pathological entities are essential. Here, we report the synthesis of thiophene-based donor-acceptor-donor heptameric ligands that can be utilized for spectral assignment of distinct amyloid-β (Aβ) aggregates, one of the pathological hallmarks in Alzheimer's disease. The ability of the ligands to selectively distinguish Aβ deposits was abolished when the chemical composition of the ligands was altered. Our findings provide the structural and functional basis for the development of new fluorescent ligands that can distinguish between aggregated proteinaceous species consisting of the same peptide or protein. In addition, such ligands might aid in interpreting the potential role of polymorphic Aβ deposits in the pathogenesis of Alzheimer's disease.
蛋白质沉积物与许多破坏性疾病有关,能够将这些病理实体可视化的荧光配体是必不可少的。在这里,我们报告了噻吩基给体-受体-给体七聚体配体的合成,该配体可用于光谱分配不同的淀粉样β(Aβ)聚集体,这是阿尔茨海默病的病理标志之一。当改变配体的化学成分时,配体选择性区分 Aβ沉积物的能力被消除。我们的发现为开发新的荧光配体提供了结构和功能基础,这些配体可以区分由相同肽或蛋白质组成的聚集蛋白物质。此外,此类配体可能有助于解释多态 Aβ沉积物在阿尔茨海默病发病机制中的潜在作用。