Bimane-based fluorescent probes with turn-on fluorescence in the presence of α-synuclein, a known hallmark of Altzeimer’s and Parkinson’s diseases. Problem: Small fluorogenic probes with high sensitivity and selectivity are powerful tools for studying the accumulation of amyloid fibrils in cells or tissue samples from patients with Alzheimer's disease (AD), Parkinson's disease (PD), and many neurodegenerative disorders. Thioflavin-T (ThT) is a widely used dye for staining amyloid fibrils because its binding to amyloid fibrils increases its fluorescence intensity. However, ThT has a relatively small Stokes shift (50 nm), which is problematic when combined with other spectrally similar molecules. It also has poor selectivity for fibrils over other aggregates, and poor cellular uptake. Solution: Bimane-based fluorescent probes that exhibit turn-on fluorescence in the presence of AD/PD biomarkers with good cellular uptake and without binding to other fibrils, allowing for early, facile, rapid detection of AD/PD and other neurodegenerative diseases. Technology: A synthetic route that enables rapid access to fluorescent probes from bimane chromophores, which show good fluorescent turn-on and selectivity among fibril types. The current probes can detect amplified fibrils (AFs) from patient tissues, while the previous method, ThT, cannot detect them effectively. In addition, the probes have large Stokes shifts in the presence of pre-formed fibrils (PFFs) and low background fluorescence in cell lysate, making them a potential PD/AD biomarker. Advantages:
Stage of Development:
Synthesis of bimane fluorescent probes with tunable emission for the detection of α-synuclein, a known hallmark of Altzeimer’s and Parkinson’s diseases. Intellectual Property:
Reference Media:
Desired Partnerships:
Docket: 23-10337