| Literature DB >> 26218347 |
Chai Lean Teoh1, Dongdong Su1, Srikanta Sahu1, Seong-Wook Yun1, Eleanor Drummond, Frances Prelli, Sulgi Lim2, Sunhee Cho2, Sihyun Ham2, Thomas Wisniewski, Young-Tae Chang1,3.
Abstract
Aggregation of amyloid β-peptide (Aβ) is implicated in the pathology of Alzheimer's disease (AD), with the soluble, Aβ oligomeric species thought to be the critical pathological species. Identification and characterization of intermediate species formed during the aggregation process is crucial to the understanding of the mechanisms by which oligomeric species mediate neuronal toxicity and following disease progression. Probing these species proved to be extremely challenging, as evident by the lack of reliable sensors, due to their heterogeneous and transient nature. We describe here an oligomer-specific fluorescent chemical probe, BoDipy-Oligomer (BD-Oligo), developed through the use of the diversity-oriented fluorescent library approach (DOFLA) and high-content, imaging-based screening. This probe enables dynamic oligomer monitoring during fibrillogenesis in vitro and shows in vivo Aβ oligomers staining possibility in the AD mice model.Entities:
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Year: 2015 PMID: 26218347 PMCID: PMC4756585 DOI: 10.1021/jacs.5b06190
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419