| Literature DB >> 31274302 |
Kaixiang Zhou1, Chang Yuan1, Bin Dai2, Kan Wang2, Yimin Chen1, Denglei Ma3, Jiapei Dai4, Yi Liang2, Hongwei Tan1, Mengchao Cui1.
Abstract
The early noninvasive diagnosis of Alzheimer's disease targeted β-amyloid (Aβ) plaques or Tau tangles is a major challenge because of the coshared β-sheet structure of the target. In contrast to tailoring probes to specific amyloids, here, we showed that near-infrared (NIR) environment-sensitive probe 18 could fluorescently discriminate Aβ and Tau from artificial aggregates to pathological change in the brain tissue. The biological evaluation demonstrated that the substantial fluorescence enhancement, large blueshift in the emission upon interactions with the aggregates, and the high binding affinity significantly contributed to the fluorescent discrimination. A simplified Ooshika-Lippert-Mataga equation provided an effective means of correlating 18 with the static relative permittivity (ε0) of proteins, elucidating the origin of the distinction capabilities, and quantitatively estimating the dielectric properties of proteins. Moreover, 18 possessed high bioavailability, including sufficient blood-brain barrier penetration, in vivo NIR imaging, and ex vivo histology in living mice.Entities:
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Year: 2019 PMID: 31274302 DOI: 10.1021/acs.jmedchem.9b00672
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446