The calpain system originally comprised three molecules: two Ca2+-dependent proteases, mu-calpain and m-calpain, and a third polypeptide, calpastatin, whose only known function is to inhibit the two calpains. Both mu- and m-calpain are heterodimers containing an identical 28-kDa subunit and an 80-kDa subunit that shares 55-65% sequence homology between the two proteases. The crystallographic structure of m-calpain reveals six "domains" in the 80-kDa subunit: 1). a 19-amino acid NH2-terminal sequence; 2). and 3). two domains that constitute the active site, IIa and IIb; 4). domain III; 5). an 18-amino acid extended sequence linking domain III to domain IV; and 6). domain IV, which resembles the penta EF-hand family of polypeptides. The single calpastatin gene can produce eight or more calpastatin polypeptides ranging from 17 to 85 kDa by use of different promoters and alternative splicing events. The physiological significance of these different calpastatins is unclear, although all bind to three different places on the calpain molecule; binding to at least two of the sites is Ca2+ dependent. Since 1989, cDNA cloning has identified 12 additional mRNAs in mammals that encode polypeptides homologous to domains IIa and IIb of the 80-kDa subunit of mu- and m-calpain, and calpain-like mRNAs have been identified in other organisms. The molecules encoded by these mRNAs have not been isolated, so little is known about their properties. How calpain activity is regulated in cells is still unclear, but the calpains ostensibly participate in a variety of cellular processes including remodeling of cytoskeletal/membrane attachments, different signal transduction pathways, and apoptosis. Deregulated calpain activity following loss of Ca2+ homeostasis results in tissue damage in response to events such as myocardial infarcts, stroke, and brain trauma.

The Calpain System

The goal of this review is to present a comprehensive survey of the many intriguing facets of creatine (Cr) and creatinine metabolism, encompassing the pathways and regulation of Cr biosynthesis an...

http://www.afboard.com/library/creatinemetabolism.pdf

Creatine and Creatinine Metabolism

We show nanoscale phase stabilization of CsPbI 3 quantum dots (QDs) to low temperatures that can be used as the active component of efficient optoelectronic devices. CsPbI 3 is an all-inorganic analog to the hybrid organic cation halide perovskites, but the cubic phase of bulk CsPbI 3 (α-CsPbI 3 )—the variant with desirable band gap—is only stable at high temperatures. We describe the formation of α-CsPbI 3 QD films that are phase-stable for months in ambient air. The films exhibit long-range electronic transport and were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.23 volts and efficiency of 10.77%. These devices also function as light-emitting diodes with low turn-on voltage and tunable emission.

http://science.sciencemag.org/content/sci/354/6308/92.full.pdf

Quantum dot-induced phase stabilization of α-CsPbI3 perovskite for high-efficiency photovoltaics.

Heavy metal removal from water/wastewater by nanosized metal oxides: a review.

Cerium dioxide (CeO2, ceria) is becoming an ubiquitous constituent in catalytic systems for a variety of applications. 2016 sees the 40th anniversary since ceria was first employed by Ford Motor Company as an oxygen storage component in car converters, to become in the years since its inception an irreplaceable component in three-way catalysts (TWCs). Apart from this well-established use, ceria is looming as a catalyst component for a wide range of catalytic applications. For some of these, such as fuel cells, CeO2-based materials have almost reached the market stage, while for some other catalytic reactions, such as reforming processes, photocatalysis, water-gas shift reaction, thermochemical water splitting, and organic reactions, ceria is emerging as a unique material, holding great promise for future market breakthroughs. While much knowledge about the fundamental characteristics of CeO2-based materials has already been acquired, new characterization techniques and powerful theoretical methods are dee...

Fundamentals and Catalytic Applications of CeO2-Based Materials

Anomalous lattice expansions have been measured for the first time in monodisperse ${\mathrm{CeO}}_{2\ensuremath{-}x}$ nanoparticles and in ${\mathrm{BaTiO}}_{3}$ single nanoparticles by electron diffraction. X-ray photoelectron spectroscopy studies on ${\mathrm{CeO}}_{2\ensuremath{-}x}$ nanoparticles and ab initio computer simulation on ${\mathrm{BaTiO}}_{3}$ clusters show that the origin of expansion is the decrease of electrostatic force caused by valence reduction of Ce ions and the increase in ionicity of Ti ions, respectively. The lattice constant change of oxide (ionic) nanoparticles with the increase in ionicity would depend on the structure of the particles. Hence, first-principles calculations of large ionic clusters are indispensable.

Origin of anomalous lattice expansion in oxide nanoparticles

Structural study on monosize CeO2-x nano-particles

Lattice relaxation of monosize CeO2-x nanocrystalline particles

Nanocrystalline barium titanate particles are prepared by the alkoxide method. The lattice constants are obtained from the electron diffraction patterns for various orientations of single particles in the size range of 15--250 nm in diameter. The present result indicates that the structural change from a tetragonal (ferroelectric) phase to a cubic (paraelectric) one occurs around 80 nm in diameter, which is in good agreement with a critical diameter recently reported. Large lattice expansions of more than 2.5% are detected in the particles down to 15 nm in diameter. The origin of the expansion is discussed on the basis of x-ray photoelectron spectroscopic analyses and a computer simulation.

Critical size and anomalous lattice expansion in nanocrystalline BaTiO 3 particles

Blueshifts in the ultraviolet absorption spectra have been observed in cerium oxide nanocrystallites. The mechanism of the absorption is a charge-transfer optical transition. The relationships among the blueshift, valence state of cerium ions, and the particle size are formulated. The blueshifts are well explained for diameters down to less than a few nanometers by the change in the electronic band structure.

Shin Tsunekawa

Papers

Origin of anomalous lattice expansion in oxide nanoparticles

Structural study on monosize CeO2-x nano-particles

Lattice relaxation of monosize CeO2-x nanocrystalline particles

Critical size and anomalous lattice expansion in nanocrystalline BaTiO 3 particles

Blueshifts in the ultraviolet absorption spectra of cerium oxide nanocrystallites