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Tatsuyuki Yoshii

Researcher at Nagoya Institute of Technology

Publications -  28
Citations -  1277

Tatsuyuki Yoshii is an academic researcher from Nagoya Institute of Technology. The author has contributed to research in topics: Protein subcellular localization prediction & Chemical biology. The author has an hindex of 12, co-authored 26 publications receiving 1061 citations. Previous affiliations of Tatsuyuki Yoshii include University of Massachusetts Amherst & Nagoya University.

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Installing logic-gate responses to a variety of biological substances in supramolecular hydrogel–enzyme hybrids

TL;DR: It is shown that redox-responsive peptide-based hydrogels have the ability to encapsulate enzymes and still retain their activities and Boolean logic gates were built into the hydrogel-enzyme hybrid materials, which were able to sense simultaneously plural specific biochemicals and execute a controlled drug release in accordance with the logic operation.
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Rational Molecular Design of Stimulus‐Responsive Supramolecular Hydrogels Based on Dipeptides

TL;DR: According to this simple design strategy, this work successfully developed three different types of oxidation-, reduction-, or photo-responsive supramolecular hydrogelators.
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In situ real-time imaging of self-sorted supramolecular nanofibres

TL;DR: In situ real-time imaging of self-sorted supramolecular nanofibre hydrogels consisting of a peptide gelator and an amphiphilic phosphate showed that the two types of fibre have different formation rates and that their respective physicochemical properties remain intact in the gel.
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Montmorillonite−Supramolecular Hydrogel Hybrid for Fluorocolorimetric Sensing of Polyamines

TL;DR: The hybridization of a supramolecular hydrogel with a layered inorganic host adsorbing a fluorescent dye produces a fluorocolorimetric sensor for spermine and spermidine, important biomarkers for cancers, in artificial urine.
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Chemically Reactive Supramolecular Hydrogel Coupled with a Signal Amplification System for Enhanced Analyte Sensitivity

TL;DR: The nanostructure and mechanical strength of the hybrid BPmoc-F3 gel were not substantially diminished by incorporation of these multiple components in the absence of target biomarkers, but could be destroyed by addition of the biomarker through the multiple enzymatic and chemical cascade reactions operating within the gel matrix.