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Detection and Imaging of Abeta1-42 and Tau Fibrils by Redesigned Fluorescent X-34 Analogues
We revisited the Congo red analogue 2,5-bis(4?-hydroxy-3?-carboxy-styryl)benzene (X-34) to develop this highly fluorescent amyloid dye for imaging Alzheimer’s disease (AD) pathology comprising Abeta and Tau fibrils. A selection of ligands with distinct optical properties were synthesized by replacing the central benzene unit of X-34, with other heterocyclic moieties. Full photophysical characterization was performed, including recording absorbance and fluorescence spectra, Stokes shift, quantum yield and fluorescence lifetimes. All ligands displayed high affinity towards recombinant amyloid fibrils of Abeta1-42 (13?300 nm Kd) and Tau (16?200 nm Kd) as well as selectivity towards the corresponding disease-associated protein aggregates in AD tissue. We observed that these ligands efficiently displaced X-34, but not Pittsburgh compound B (PiB) from recombinant Abeta1-42 amyloid fibrils, arguing for retained targeting of the Congo red type binding site. We foresee that the X-34 scaffold offers the possibility to develop novel high-affinity ligands for Abeta pathology found in human AD brain in a different mode compared with PiB, potentially recognizing different polymorphs of Abeta fibrils.
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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2054 | ChemSpider