Department of Physics, Chemistry and Biology, Linköping University, 581 83, Linköping, Sweden.
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, 46202, Indiana, USA.
Chemistry. 2022 Nov 7;28(62):e202201557. doi: 10.1002/chem.202201557. Epub 2022 Sep 5.
Protein deposits composed of specific proteins or peptides are associated with several neurodegenerative diseases and fluorescent ligands able to detect these pathological hallmarks are vital. Here, we report the synthesis of a class of thiophene-based ligands, denoted proteophenes, with different amino acid side-chain functionalities along the conjugated backbone, which display selectivity towards specific disease-associated protein aggregates in tissue sections with Alzheimer's disease (AD) pathology. The selectivity of the ligands towards AD associated pathological hallmarks, such as aggregates of the amyloid-β (Aβ) peptide or tau filamentous inclusions, was highly dependent on the chemical nature of the amino acid functionality, as well as on the location of the functionality along the pentameric thiophene backbone. Finally, the concept of synthesizing donor-acceptor-donor proteophenes with distinct photophysical properties was shown. Our findings provide the structural and functional basis for the development of new thiophene-based ligands that can be utilized for optical assignment of different aggregated proteinaceous species in tissue sections.
由特定蛋白质或肽组成的蛋白质沉积物与几种神经退行性疾病有关,能够检测这些病理标志物的荧光配体至关重要。在这里,我们报告了一类噻吩基配体的合成,这些配体表示为 proteophenes,它们在共轭主链上具有不同的氨基酸侧链官能团,在具有阿尔茨海默病 (AD) 病理学的组织切片中对特定与疾病相关的蛋白质聚集体具有选择性。配体对 AD 相关病理标志物的选择性,例如淀粉样β (Aβ) 肽或 tau 丝状包涵体的聚集,高度依赖于氨基酸官能团的化学性质,以及官能团在五聚噻吩主链上的位置。最后,展示了合成具有不同光物理性质的供体-受体-供体 proteophenes 的概念。我们的研究结果为开发新的噻吩基配体提供了结构和功能基础,这些配体可用于在组织切片中光学分配不同的聚集蛋白质物质。