171 research outputs found

    Understanding and Implementing Extended Saxophone Techniques

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    Contemporary classical music often pushes the boundaries of how instruments should be played and what kinds of sounds they should produce. A great deal of contemporary music requires the player to utilize playing techniques that may seem very strange and difficult to those who are unfamiliar with them. These unusual practices, known as extended techniques, can include playing in extreme ranges, manipulating pitches in particular ways, and applying abnormal articulations. While once seen as a sort of novelty, these extended techniques are becoming increasingly essential to the contemporary musician. This is especially true of the saxophonist. While nearly every other major instrument was developed gradually over extremely long periods of time, the saxophone was explicitly invented in 1841. As such, a relatively high percentage of saxophone literature was written in the twentieth century and beyond. It is this contemporary literature that frequently demands the use of the aforementioned extended techniques. It is crucial for the modern saxophonist to have at least a basic understanding of these techniques in order to approach much of this literature. This project discusses the implication of several extended techniques that commonly occur throughout the saxophone repertoire. The extended techniques covered include playing in the altissimo register, pitch bending, double tonguing, flutter tonguing, slap tonguing, growling, playing multiphonic pitches, and circular breathing

    Computationally designed libraries of fluorescent proteins evaluated by preservation and diversity of function

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    To determine which of seven library design algorithms best introduces new protein function without destroying it altogether, seven combinatorial libraries of green fluorescent protein variants were designed and synthesized. Each was evaluated by distributions of emission intensity and color compiled from measurements made in vivo. Additional comparisons were made with a library constructed by error-prone PCR. Among the designed libraries, fluorescent function was preserved for the greatest fraction of samples in a library designed by using a structure-based computational method developed and described here. A trend was observed toward greater diversity of color in designed libraries that better preserved fluorescence. Contrary to trends observed among libraries constructed by error-prone PCR, preservation of function was observed to increase with a library's average mutation level among the four libraries designed with structure-based computational methods

    On the construction and sustainability of happiness: Where does my happiness come from?

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    Problem. Happiness is attributed to three sources: genetics and personality (50%), the situation (10%), and voluntary behaviors (40%) (Lyubomirsky, 2008). Few studies exist on the subject of happiness factors, their duration, and how these factors may relate to Lyubomirsky\u27s (2008) three sources of happiness, the purpose of this study. Method. Three hundred and forty-seven undergraduates listed what they felt contributed to their overall happiness. Then they indicated the three items they considered the most significant contributors. Finally, participants reported the duration (e.g., minutes, hours, days, weeks, or years) of happiness caused by each of these items. Results and Discussion. The number of happiness items participants expressed ranged from 0 to 77 (M = 28.58; SD = 13.74). The item listed most often was family (20.27%) followed by friends (15.18%). Most people gave priority to items that made them happy for years. As priority of the items decreased so did duration suggesting that people place greater value on factors that lead to prolonged levels of happiness. These findings have implications for happiness construction and sustainability as increasing individuals\u27 happiness levels may involve seeking out more socially-beneficial--as well as longer-lasting--resources

    Redefining happiness: Is the happiness pie literature missing some slices?

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    This study examined the relationships among happiness-related factors, as well as the relation between the antecedents of happiness (e.g., an individual\u27s personality, situations, and voluntary behavior) and self-reported individual differences. Three hundred forty-seven undergraduates completed measures of happiness, positive affect, subjective well-being, contentment, self-compassion, depression, neuroticism, mindfulness, and openness to experience. Participants also indicated the percentage of their happiness due to personality, the situation, and voluntary behaviors. The results corroborate evidence for happiness being most indicative of a multidimensional construct, as contentment, subjective well-being, and happiness were highly related. Additionally, in spite of research showing that almost half of our happiness is determined by voluntary actions, participants, on average, divided the happiness pie into thirds, attributing their happiness to personality (30.36%), the situation (36.88%), and voluntary actions (32.7%)

    Greek community needs assessment: Reducing the negative impact of alcohol and drugs

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    Participants representing Clemson\u27s Greek community have designed a research project that aims to define the problems associated with alcohol and drug misuse in the Greek community at Clemson University and to implement action steps based on sound evidence to mitigate the negative consequences associated with that misuse. The team is made up of Greek student leaders who are passionate about making a difference in their community and ultimately creating a plan to reduce alcohol and drug abuse among members. The team has conducted IRB and National PanHellenic approved focus groups and is in the process of coding the data. This poster reflects a preliminary analysis of that data

    Transmission electron microscopy characterization of fluorescently labelled amyloid β 1-40 and α-synuclein aggregates

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    <p>Abstract</p> <p>Background</p> <p>Fluorescent tags, including small organic molecules and fluorescent proteins, enable the localization of protein molecules in biomedical research experiments. However, the use of these labels may interfere with the formation of larger-scale protein structures such as amyloid aggregates. Therefore, we investigate the effects of some commonly used fluorescent tags on the morphologies of fibrils grown from the Alzheimer's disease-associated peptide Amyloid β 1-40 (Aβ40) and the Parkinson's disease-associated protein α-synuclein (αS).</p> <p>Results</p> <p>Using transmission electron microscopy (TEM), we verify that N-terminal labeling of Aβ40 with AMCA, TAMRA, and Hilyte-Fluor 488 tags does not prevent the formation of protofibrils and amyloid fibrils of various widths. We also measure the two-photon action cross-section of Aβ40 labelled with Hilyte Fluor 488 and demonstrate that this tag is suitable for use with two-photon fluorescence techniques. Similarly, we find that Alexa Fluor 488 labelling of αS variant proteins near either the N or C terminus (position 9 or 130) does not interfere with the formation of amyloid and other types of αS fibrils. We also present TEM images of fibrils grown from αS C-terminally labelled with enhanced green fluorescent protein (EGFP). Near neutral pH, two types of αS-EGFP fibrils are observed via TEM, while denaturation of the EGFP tag leads to the formation of additional species.</p> <p>Conclusions</p> <p>We demonstrate that several small extrinsic fluorescent tags are compatible with studies of amyloid protein aggregation. However, although fibrils can be grown from αS labelled with EGFP, the conformation of the fluorescent protein tag affects the observed aggregate morphologies. Thus, our results should assist researchers with label selection and optimization of solution conditions for aggregation studies involving fluorescence techniques.</p

    Protein-retention expansion microscopy of cells and tissues labeled using standard fluorescent proteins and antibodies

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    Expansion microscopy (ExM) enables imaging of preserved specimens with nanoscale precision on diffraction-limited instead of specialized super-resolution microscopes. ExM works by physically separating fluorescent probes after anchoring them to a swellable gel. The first ExM method did not result in the retention of native proteins in the gel and relied on custom-made reagents that are not widely available. Here we describe protein retention ExM (proExM), a variant of ExM in which proteins are anchored to the swellable gel, allowing the use of conventional fluorescently labeled antibodies and streptavidin, and fluorescent proteins. We validated and demonstrated the utility of proExM for multicolor super-resolution (~70 nm) imaging of cells and mammalian tissues on conventional microscopes.United States. National Institutes of Health (1R01GM104948)United States. National Institutes of Health (1DP1NS087724)United States. National Institutes of Health ( NIH 1R01EY023173)United States. National Institutes of Health (1U01MH106011

    Towards a Clinically Relevant Lentiviral Transduction Protocol for Primary Human CD34+ Hematopoietic Stem/Progenitor Cells

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    Background: Hematopoietic stem cells (HSC), in particular mobilized peripheral blood stem cells, represent an attractive target for cell and gene therapy. Efficient gene delivery into these target cells without compromising self-renewal and multipotency is crucial for the success of gene therapy. We investigated factors involved in the ex vivo transduction of CD34 + HSCs in order to develop a clinically relevant transduction protocol for gene delivery. Specifically sought was a protocol that allows for efficient transduction with minimal ex vivo manipulation without serum or other reagents of animal origin. Methodology/Principal Findings: Using commercially available G-CSF mobilized peripheral blood (PB) CD34 + cells as the most clinically relevant target, we systematically examined factors including the use of serum, cytokine combinations, prestimulation time, multiplicity of infection (MOI), transduction duration and the use of spinoculation and/or retronectin. A self-inactivating lentiviral vector (SIN-LV) carrying enhanced green fluorescent protein (GFP) was used as the gene delivery vehicle. HSCs were monitored for transduction efficiency, surface marker expression and cellular function. We were able to demonstrate that efficient gene transduction can be achieved with minimal ex vivo manipulation while maintaining the cellular function of transduced HSCs without serum or other reagents of animal origin. Conclusions/Significance: This study helps to better define factors relevant towards developing a standard clinical protocol for the delivery of SIN-LV into CD34 + cells
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