50 research outputs found

    Technological advancements in the analysis of human motion and posture management through digital devices

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    Technological development of motion and posture analyses is rapidly progressing, especially in rehabilitation settings and sport biomechanics. Consequently, clear discrimination among different measurement systems is required to diversify their use as needed. This review aims to resume the currently used motion and posture analysis systems, clarify and suggest the appropriate approaches suitable for specific cases or contexts. The currently gold standard systems of motion analysis, widely used in clinical settings, present several limitations related to marker placement or long procedure time. Fully automated and markerless systems are overcoming these drawbacks for conducting biomechanical studies, especially outside laboratories. Similarly, new posture analysis techniques are emerging, often driven by the need for fast and non-invasive methods to obtain high-precision results. These new technologies have also become effective for children or adolescents with non-specific back pain and postural insufficiencies. The evolutions of these methods aim to standardize measurements and provide manageable tools in clinical practice for the early diagnosis of musculoskeletal pathologies and to monitor daily improvements of each patient. Herein, these devices and their uses are described, providing researchers, clinicians, orthopedics, physical therapists, and sports coaches an effective guide to use new technologies in their practice as instruments of diagnosis, therapy, and prevention

    Proteomic dataset of Paracentrotus lividus gonads of different sexes and at different maturation stages

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    We report the proteomic dataset of gonads from wild Paracentrotus lividus related to the research article entitled "Proteomic changes occurring along gonad maturation in the edible sea urchin Paracentrotus lividus" [1]. Gonads of three individuals per sex in the recovery, pre-mature, mature, and spent stages were analyzed using a shotgun proteomics approach based on filter-aided sample preparation followed by tandem mass spectrometry, protein identification carried out using Sequest-HT as the search engine within the Proteome Discoverer informatics platform, and label-free differential analysis. The dataset has been deposited in the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PRIDE: PXD004200

    Pedicled flaps for anterior chest wall reconstruction

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    Pedicled local or regional flaps are the main reconstructive tool for chest wall defects. Muscle or musculocutaneous flaps are most commonly used, with the latissimus dorsi and the pectoralis major being the workhorse flaps. However, perforator flaps have recently affirmed even for reconstruction of complex defects. A thorough knowledge of the vascular anatomy of the thorax and of the patient’s medical history is essential for selecting the best reconstructive option. The defect location, size, and depth as well as previous surgeries in the same area are the main issues affecting the reconstructive choices

    Characterization of size and composition of milk fat globules from Sarda and Saanen dairy goats

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    The small size of goat milk fat globules (MFGs) is one of the factors contributing to the higher digestibility of goat milk compared to other milks. In this study, size, protein composition and lipid distribution of MFGs were evaluated comparatively in a popular dairy breed, Saanen, and in a minor breed, Sarda. MFGs were found to be significantly smaller in Sarda compared to Saanen goats, with average diameters of 2.73 \ub1 0.15 \u3bcm and 3.63 \ub1 0.27 \u3bcm, respectively. Raman spectroscopy revealed differences in the lipid profiles of differently sized MFGs within each breed, with MFGs of the same size class having comparable profiles between breeds. Proteomic characterization by SDS-PAGE followed by tandem mass spectrometry (GeLC-MS/MS) and label-free differential quantification highlighted significant differences in expression levels of MFG proteins from the two breeds, with a higher abundance of cytoplasmic proteins in Sarda MFGs and of membrane proteins in Saanen MFGs. Moreover, differences in the relative abundance of several major MFG proteins were observed for the two breeds. In conclusion, this study demonstrates the existence of breed-dependent differences in the lipid and protein makeup of goat MFGs, likely related to their different size distribution. This highlights once again the importance of investigating biodiversity in autochthonous and neglected breeds, which often possess valuable attributes that might be lost as a consequence of the widespread diffusion of highly productive, but more homogeneous, dairy breeds

    Differences in the peptide profile of raw and pasteurised ovine milk cheese and implications for its bioactive potential

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    Cheese produced using raw ovine milk (R) or pasteurised ovine milk (P) was subjected to peptide extraction, characterisation by mass spectrometry and bioinformatic analysis with the aim of assessing the impact of milk pasteurisation on the final peptide profile. In total, 187 peptides arising from \u3b2-casein, \u3b1S1-casein, and \u3b1S2-casein were identified. Upon label-free quantitation, 58 peptides were found to be significantly different in the two preparations; 38 were more abundant in R and 20 were more abundant in P. Of these, 27 were unique to R and 10 were unique to P. Bioinformatic analysis by EnzymePredictor provided insights into the influence of milk pasteurisation on susceptibility of cheese proteins to proteolytic enzymes during ripening. Finally, BIOPEP analysis predicted a biological activity for 37 of the 187 identified sequences (20%), with a significantly higher abundance of peptides with immunomodulating and ACE-inhibitor properties in R cheeses

    Occurrence and characterization of peptaibols from Trichoderma citrinoviride, an endophytic fungus of cork oak, using electrospray ionization quadrupole time - of - flight mass spectrometry

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    A cork oak endophytic strain of Trichoderma citrinoviride, previously selected for its antagonistic potential against various fungal pathogens involved in oak decline, was screened for the production of bioactive secondary metabolites. From liquid culture a mixture of polypeptide antibiotics (peptaibols) belonging to the paracelsin family was isolated and characterized. This peptide mixture was purified by column chromatography and preparative TLC on silica gel, and separated by analytical HPLC. It was analysed by MALDI-TOF MS and nano-ESI-QTOF MS. Tandem mass experiments were performed to determine the amino acid sequences based on the fragmentation pattern of selected parent ions. The mixture comprised 20-residue peptides with C-terminal phenylalaninol and N-terminal acetylation. Twenty-eight amino acid sequences were identified, and amino acid exchanges were located in positions 6, 9, 12 and 17. Among them, seven sequences are new as compared to those reported in the database specifically for peptaibols and in the literature. In addition, we obtained experimental evidence suggesting the existence of non-covalent dimeric forms (homo- and hetero-) of the various peptaibol species. The peptide mixture showed strong antifungal activity toward seven important forest tree pathogens, and it was highly toxic in an Artemia salina (brine shrimp) bioassay. These results emphasize the cryptic role of endophytic fungi as a source of novel bioactive natural products and biocontrol agents

    Proteomic analysis of muscle tissue from gilthead sea bream (Sparus aurata, L.) farmed in offshore floating cages

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    Characterization of the muscle tissue proteome is key to many aspects of fish aquaculture, encompassing physiology, growth, food safety, seafood authentication and quality, traceability and shelf-life. In this study, a 2D-PAGE-MS study was performed on gilthead sea bream (Sparus aurata, L.) muscle tissue along the production cycle in four offshore floating cage plants and two repopulation lagoons located in different areas of Sardinia, Italy. The aim of this study was to accomplish systematic characterization of the gilthead sea bream muscle proteome, and to gather data about its variability in physiological conditions occurring in both farmed and wild fish. In general, a relatively stable protein expression pattern was observed in farmed sea bream muscle compared to other more dynamic tissue proteomes, such as liver. However, several statistically significant variations in abundance of some proteins and their isoforms were detected, related to growth and environmental factors. Among these, parvalbumins, troponins, and Wap65 showed variations according to fish length and water temperature. Interestingly, the ratio of structural proteins versus glycolytic enzymes was also observed to change during the production cycle, showing an increase with fish length. In order to assess whether the farming conditions were able to induce alterations in the muscle proteome, farmed and wild fish were subjected to a differential proteomics analysis. The data gathered in this study indicate that the protein expression profile of muscle tissue is comparable in wild and maricultured gilthead sea breams of commercial size, supporting the view that farming in offshore floating cages might favor proper muscle tissue development, and therefore enable the production of higher quality fish.In conclusion, this work describes the detailed characterization of the sea bream muscle proteome, and provides a number of insights on its size and environment-related variability
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