Amyotrophic lateral sclerosis (ALS) is a heterogeneous motor neuron disease for which no effective treatment is available, despite decades of research into SOD1-mutant familial ALS (FALS). The majority of ALS patients have no familial history, making the modeling of sporadic ALS (SALS) essential to the development of ALS therapeutics. However, as mutations underlying ALS pathogenesis have not yet been identified, it remains difficult to establish useful models of SALS. Using induced pluripotent stem cell (iPSC) technology to generate stem and differentiated cells retaining the patients' full genetic information, we have established a large number of in vitro cellular models of SALS. These models showed phenotypic differences in their pattern of neuronal degeneration, types of abnormal protein aggregates, cell death mechanisms, and onset and progression of these phenotypes in vitro among cases. We therefore developed a system for case clustering capable of subdividing these heterogeneous SALS models by their in vitro characteristics. We further evaluated multiple-phenotype rescue of these subclassified SALS models using agents selected from non-SOD1 FALS models, and identified ropinirole as a potential therapeutic candidate. Integration of the datasets acquired in this study permitted the visualization of molecular pathologies shared across a wide range of SALS models.

We review the syntheses, optical properties, and biological applications of cadmium selenide (CdSe) and cadmium selenide-zinc sulfide (CdSe-ZnS) quantum dots (QDs) and gold (Au) and silver (Ag) nanoparticles (NPs). Specifically, we selected the syntheses of QDs and Au and Ag NPs in aqueous and organic phases, size- and shape-dependent photoluminescence (PL) of QDs and plasmon of metal NPs, and their bioimaging applications. The PL properties of QDs are discussed with reference to their band gap structure and various electronic transitions, relations of PL and photoactivated PL with surface defects, and blinking of single QDs. Optical properties of Ag and Au NPs are discussed with reference to their size- and shape-dependent surface plasmon bands, electron dynamics and relaxation, and surface-enhanced Raman scattering (SERS). The bioimaging applications are discussed with reference to in vitro and in vivo imaging of live cells, and in vivo imaging of cancers, tumor vasculature, and lymph nodes. Other aspects of the review are in vivo deep tissue imaging, multiphoton excitation, NIR fluorescence and SERS imaging, and toxic effects of NPs and their clearance from the body.

Bioconjugated nanomaterials offer endless opportunities to advance both nanobiotechnology and biomedical technology. In this regard, semiconductor nanoparticles, also called quantum dots, are of particular interest for multimodal, multifunctional and multiplexed imaging of biomolecules, cells, tissues and animals. The unique optical properties, such as size-dependent tunable absorption and emission in the visible and NIR regions, narrow emission and broad absorption bands, high photoluminescence quantum yields, large one- and multi-photon absorption cross-sections, and exceptional photostability are the advantages of quantum dots. Multimodal imaging probes are developed by interfacing the unique optical properties of quantum dots with magnetic or radioactive materials. Besides, crystalline structure of quantum dots adds scope for high-contrast X-ray and TEM imaging. Yet another unique feature of a quantum dot is its spacious and flexible surface which is promising to integrate multiple ligands and antibodies and construct multi-functional probes for bioimaging. In this critical review, we will summarize recent advancements in the preparation of biocompatible quantum dots, bioconjugation of quantum dots, and applications of quantum dots and their bioconjugates for targeted and nonspecific imaging of extracellular and intracellular proteins, organelles and functions (181 references).

Local electric field and scattering cross section on Ag nanoparticles were evaluated by the FDTD (finite difference time domain) method with respect to single-molecule sensitivity (SMS) in SERS (surface-enhanced Raman scattering). As a result, (1) vast enhancement of >300-fold (in amplitude enhancement) in the SMS level was obtained at a junction between two connecting Ag particles with various shapes and sizes in addition to an edge of isolated triangular cylinders. Other sites of the connecting particles and of isolated circular and ellipsoidal cylinders gave only modest enhancement of ca. 20-30-fold. (2) The enormously large electric field at the junction rapidly decays with increasing gap sizes <1 nm, irrespective of particle size or shape. In contrast, the LSP (localized surface plasmon) extinction spectra from connecting particles gradually shift toward those from isolated particles with the gap. Thus, in addition to the dipole LSP excitation, nanostructures such as sharp edges, which yield higher order surface modes, are crucial for the vast enhancement. Twodimensional ordered structures do not yield any additional enhancement concerning SMS-SERS. (3) A red shift of the LSP extinction peak with decreasing height of Ag particles was reproduced only by use of threedimensional simulation, while broadening and larger extinction at longer wavelength are given by two-dimensional calculation. (4) Blinking of SERS signal observed for dye and DNA base is most probably due to thermal diffusion of adsorbates between the junction with vast enhancement and ordinary sites with modest enhancement, which was supported by the numerical simulation and also experimentally evidenced by suppression of the phenomena at low temperature.