Haptic influences on Chopin pianism: case studies from the music of Szymanowska and Kessler

What makes Fryderyk Chopin (1810-1849), one of the most revered and loved composers in the piano repertoire, and is he truly a unique figure? This question has driven me for most of my musical life, resulting in my current research. This project emerged from my fascination with the wealth of forgotten composers and their music, which seemed all so familiar - was Chopin influenced by them to a degree that was never documented or questioned before? While Szymanowska’s influence has been noted before, the haptic considerations that led this process of influence have not been investigated. Using my experience as a pianist, I approached this question through a haptic lens. This thesis is divided into an Introduction, which addresses my motivation, Chapter 1, which refers to the historiographical and musical background of Chopin’s formative years, the practice-as research approach to the methodology, and the literature review. Chapter 2 focuses primarily on two composers: Maria Agata Szymanowska (1789–1831) and Joseph Christoph Kessler (1800-1871). I compare their preludes and etudes, through a haptic perspective, with the preludes and etudes of Chopin. The influence of Szymanowska and Kessler on Chopin is demonstrated, through the presence of clearly identifiable haptic characteristics. The musical examples are integrated with video clips that demonstrate the haptic connections, in each case, at the piano. The last section of the thesis discusses my reflection and conclusion that Chopin was indeed influenced by these composers, especially through the haptic process. Although Chopin later developed his style beyond the formative influence of Kessler and Syzmanowska, I believe his music, and his approach to piano writing, owes a substantial debt to these two lesser-known composers, and that this connection can only be truly identified through the investigation of haptic considerations

Ligand-Protected Gold Clusters

Small gold clusters with diameters less than or equal to 2 nm (below approximately 200 atoms) possess geometric and electronic structures different from bulk gold. When these gold clusters are protected by ligands, these clusters can be treated as chemical compounds. This review focuses on gold clusters protected by chalcogenate (thiolate, selenolate, or tellurolate) ligands and describes the methods by which these clusters are synthesized as well as their geometric/electronic structures and physical and chemical properties. Recent findings regarding ligand exchange reactions, which may be used to impart functionality to these compounds, are also described

Structural and functional analyses of calcium ion response factors in the mantle of Pinctada fucata

The pearl oyster, Pinctada fucata, is cultured for pearl production in Japan. The shell of the pearl oyster consists of calcium carbonate and a small amount of organic matrix. Despite many studies of the shell matrix proteins, the mechanism by which calcium elements are transported from the mantle to the shell remains unclear. Investigating the molecular mechanism of calcium transportation, we prepared artificial seawater with a high concentration of calcium ions (10ASW) to induce calcification in the pearl oyster. When pearl oysters were cultured in 10ASW, unusual nanoparticles were precipitated on the surface of the nacreous layer. SDS-PAGE and 2D-PAGE analyses revealed that some calcium-sensing proteins (Sarcoplasmic Ca-binding Protein (Pf-SCP) and Pf-filamin A) might be related to the synthesis of these nanoparticles. The recombinant proteins of Pf-SCP can bind to calcium ions and accumulate nanoparticles of calcium carbonate crystals. However, transcriptomic analysis of the pearl oysters grown in 10ASW showed that the matrix protein genes in the shell did not differ before and after treatment with 10ASW. These results suggest that, despite increasing calcium transportation to the shell, treatment with a high concentration of calcium ions does not induce formation of the organic framework in the shell microstructure. These findings offer meaningful insights into the transportation of calcium elements from the mantle to the shell

Evidence for an Essential Deglycosylation-Independent Activity of PNGase in Drosophila melanogaster

BACKGROUND: Peptide:N-glycanase (PNGase) is an enzyme which releases N-linked glycans from glycopeptides/glycoproteins. This enzyme plays a role in the ER-associated degradation (ERAD) pathway in yeast and mice, but the biological importance of this activity remains unknown. PRINCIPAL FINDINGS: In this study, we characterized the ortholog of cytoplasmic PNGases, PNGase-like (Pngl), in Drosophila melanogaster. Pngl was found to have a molecular weight of approximately 74K and was mainly localized in the cytosol. Pngl lacks a CXXC motif that is critical for enzymatic activity in other species and accordingly did not appear to possess PNGase activity, though it still retains carbohydrate-binding activity. We generated microdeletions in the Pngl locus in order to investigate the functional importance of this protein in vivo. Elimination of Pngl led to a serious developmental delay or arrest during the larval and pupal stages, and surviving mutant adult males and females were frequently sterile. Most importantly, these phenotypes were rescued by ubiquitous expression of Pngl, clearly indicating that those phenotypic consequences were indeed due to the lack of functional Pngl. Interestingly, a putative "catalytic-inactive" mutant could not rescue the growth-delay phenotype, indicating that a biochemical activity of this protein is important for its biological function. CONCLUSION: Pngl was shown to be inevitable for the proper developmental transition and the biochemical properties other than deglycosylation activity is important for its biological function

Toxicoproteomic evaluation of carbon nanomaterials in vitro

Carbon nanotubes (CNTs) have already been successfully implemented in various fields, and they are anticipated to have innovative applications in medical science. However, CNTs have asbestos-like properties, such as their nanoscale size and high aspect ratio (> 100). Moreover, CNTs may persist in the body for a long time. These properties are thought to cause malignant mesothelioma and lung cancer. However, based on conventional toxicity assessment systems, the carcinogenicity of asbestos and CNTs is unclear. The reason for late countermeasures against asbestos is that reliable, long-term safety assessments have not yet been developed by toxicologists. Therefore, a new type of long-term safety assessment, different from the existing methods, is needed for carbon nanomaterials. Recently, we applied a proteomic approach to the safety assessment of carbon nanomaterials. In this review, we discuss the basic concept of our approach, the results, the problems, and the possibility of a long-term safety assessment for carbon nanomaterials using the toxicoproteomic approach.ArticleJournal of Proteomics. 74(12):2703-2712 (2011)journal articl