Solvatochromic peptidic binder obtained via extended phage display acts as a fluororeporter for fragment-based drug discovery (FBDD).

We have previously established a selection system to obtain a solvatochromic protein binder from a peptidic fluoroprobe library via the extended T7 phage display. Here, we use the peptidic binder as a fluororeporter in this proof-of-concept study of fragment-based screening approach to drug discovery. The binder is released from the target protein on mixing with an appropriate lead compound, thereby altering its fluorescence color/intensity under 365 nm ultraviolet wavelength irradiation. By this instant screening outcome, the affinity of the lead compound is apparent to the naked eye, and quantified with a portable microvolume fluorophotometer. We envision that our simple and affordable screening system will provide opportunities for early stage drug discovery, especially for non-experts in academia and education because expensive hardware is not required for qualifying the measurements.

High azimuthal angle tolerant dual-channel wavelength filter from visible to NIR using conically mounted guided mode resonance structures.

We present a concept to design narrow linewidth dual-channel wavelength filters using the principle of wavelength tuning under conical mounting of guided mode resonance structure. The general procedure for the design of such filters from visible to NIR wavelength range is presented and validated experimentally. We show that already fabricated guided mode resonance structures that do not show dual wavelength filtering at these wavelengths in classical mounting can exhibit dual wavelength filtering in conical mounting. Using this principle, we design high azimuthal angle tolerant guided mode resonance dual wavelength filters at C-band communication wavelengths (1310 and 1550 nm) that are insensitive to azimuthal angle over a range of up to 20 deg, achieved in expense of a tolerance in the angle of incidence that is less than 3 deg.

Magnetic-particle-sensing based diagnostic protocols and applications.

Magnetic particle-labeled biomaterial detection has attracted much attention in recent years for a number of reasons; easy manipulation by external magnetic fields, easy functionalization of the surface, and large surface-to-volume ratio, to name but a few. In this review, we report on our recent investigations into the detection of nano-sized magnetic particles. First, the detection by Hall magnetic sensor with lock-in amplifier and alternative magnetic field is summarized. Then, our approach to detect sub-200 nm diameter target magnetic particles via relatively large micoro-sized "columnar particles" by optical microscopy is described. Subsequently, we summarize magnetic particle detection based on optical techniques; one method is based on the scattering of the magnetically-assembled nano-sized magnetic bead chain in rotating magnetic fields and the other one is based on the reflection of magnetic target particles and porous silicon. Finally, we report recent works with reference to more familiar industrial products (such as smartphone-based medical diagnosis systems and magnetic removal of unspecific-binded nano-sized particles, or "magnetic washing").