Synthesis of Thiophene-Based Optical Ligands That Selectively Detect Tau Pathology in Alzheimer's Disease

被引:31
作者
Shirani, Hamid [1 ]
Appelqvist, Hanna [1 ]
Back, Marcus [1 ]
Klingstedt, Therese [1 ]
Cairns, Nigel J. [2 ]
Nilsson, K. Peter R. [1 ]
机构
[1] Linkoping Univ, Div Chem, Dept Phys Chem & Biol, S-58183 Linkoping, Sweden
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
基金
瑞典研究理事会;
关键词
Alzheimers disease; amyloid-beta; fluorescent ligands; protein aggregates; tau aggregates; AMYLOID IMAGING AGENTS; THIOFLAVIN-T; SPECTRAL ASSIGNMENT; BRAIN; FIBRILS; BINDING; BETA; PET; OLIGOTHIOPHENES; PLAQUES;
D O I
10.1002/chem.201703846
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The accumulation of protein aggregates is associated with many devastating neurodegenerative diseases and the development of molecular ligands able to detect these pathological hallmarks is essential. Here, the synthesis of thiophene based optical ligands, denoted bi-thiophene-vinyl-benzothiazoles (bTVBTs) that can be utilized for selective assignment of tau aggregates in brain tissue with Alzheimer's disease (AD) pathology is reported. The ability of the ligands to selectively distinguish tau deposits from the other AD associated pathological hallmark, senile plaques consisting of aggregated amyloid- (A) peptide, was reduced when the chemical composition of the ligands was altered, verifying that specific molecular interactions between the ligands and the aggregates are necessary for the selective detection of tau deposits. Our findings provide the structural and functional basis for the development of new fluorescent ligands that can distinguish between aggregated proteinaceous species consisting of different proteins. In addition, the bTVBT scaffold might be utilized to create powerful practical research tools for studying the underlying molecular events of tau aggregation and for creating novel agents for clinical imaging of tau pathology in AD.
引用
收藏
页码:17127 / 17135
页数:9
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