Publications by authors named "Aoi Isono"

Article Synopsis
  • Researchers created new carriers for boron neutron capture therapy (BNCT) optimized for delivering boron clusters into cells using a combination of lipopeptide and disulfide linker.
  • The carriers were designed based on a structure called pepducin, enhancing membrane permeability and tested for effectiveness in glioblastoma cells, with compound 5a showing the best results.
  • Both compounds 5a and 14 led to improved boron accumulation and more effective radiosensitization in cells compared to traditional BSH, highlighting the potential of lipopeptides for better drug delivery in BNCT.
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Mitochondria play a key role in cell survival by perfoming functions such as adenosine tri-phosphate (ATP) synthesis, regulation of apoptotic cell death, calcium storage. Hypoxic conditions induce mitochondrial dysfunction, which leads to endothelial injury in cerebral ischemia. Functional disorders include the following: collapse of mitochondrial membrane potential, reduction of ATP synthesis, and generation of reactive oxygen species (ROS).

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To elucidate the mechanisms of direct transmembrane penetration of pepducins, which are artificial lipopeptide G protein-coupled receptor (GPCR) modulators, we developed two types of FRET-based probes, Pep13-FL-SS-Dab (13) targeting the inner leaflet of the lipid bilayer and Pep13-Dab-SS-FL (14) targeting the cytosol, respectively. They are composed of a pepducin moiety and a fluorescent switch component consisting of 5(6)-carboxyfluorescein (FAM) as a fluorophore and dabcyl as a quencher connected through disulfide bond linkage. When they are internalized into the cytosol, intracellular glutathione can cleave the disulfide bond to release the quencher, which results in a turn-on fluorescence signal.

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