99 research outputs found
Measurement of the behaviour of residual gas particles on cryogenic surfaces to improve the simulation of dynamic vacuum effects
Marine organisms as source of bioactive molecules applied in restoration projects
In recent decades research in the conservation and restoration field has provided sustainable alternatives to
traditional procedures for cleaning or controlling the microbial colonization of works of art. In the present study,
for the first time novel bioactive molecules extracted from marine invertebrate organisms (Anthozoa) were tested
instead of chemical compounds for removing protein layers or as a biocide for controlling fungal or bacterial
colonization. In particular, Bioactive Molecules with Protease activity (BMP), acting in a temperature range of 4- 30\ub0C,
were tested for the hydrolysis of protein layers on laboratory specimens. The cleaning protocol provides a selective
procedure to avoid damage to the original materials constituting the heritage object.
Concurrently, enzymatic cleaning was also performed using commercial Protease from Aspergillus sojae (Type XIX),
in order to compare their hydrolytic activities. Bioactive Molecules with Antimicrobial activity (BMA1, BMA2) were
tested to control bacterial (Bacillus, Micrococcus) or fungal (Aspergillus, Penicillium) growth, previously isolated from
colonized canvas samples and characterized by an integrated approach based on in vitro culture, microscopy and
molecular investigations. These molecules were tested to define the Minimal Inhibitory Concentration (MIC) and
Minimal Bactericidal/ Fungicidal Concentration (MBC/MFC). Specifically, BMAs were used to control fungal growth
during the relining of the painting (laboratory specimens), carried out using a canvas support, and glue paste as
binder.
In our hypothesis, these molecules provide an important contribution to the development of innovative protocols
for biocleaning or microbial growth control, based on fast and easy application, operator friendly and
environmentally sustainable molecules
A variational approach to strongly damped wave equations
We discuss a Hilbert space method that allows to prove analytical
well-posedness of a class of linear strongly damped wave equations. The main
technical tool is a perturbation lemma for sesquilinear forms, which seems to
be new. In most common linear cases we can furthermore apply a recent result
due to Crouzeix--Haase, thus extending several known results and obtaining
optimal analyticity angle.Comment: This is an extended version of an article appeared in
\emph{Functional Analysis and Evolution Equations -- The G\"unter Lumer
Volume}, edited by H. Amann et al., Birkh\"auser, Basel, 2008. In the latest
submission to arXiv only some typos have been fixe
u-PAR expression in cancer associated fibroblast: new acquisitions in multiple myeloma progression
BACKGROUND: Multiple Myeloma (MM) is a B-cell malignancy in which clonal plasma cells progressively expand within the bone marrow (BM) as effect of complex interactions with extracellular matrix and a number of microenvironmental cells. Among these, cancer-associated fibroblasts (CAF) mediate crucial reciprocal signals with MM cells and are associated to aggressive disease and poor prognosis. A large body of evidence emphasizes the role of the urokinase plasminogen activator (u-PA) and its receptor u-PAR in potentiating the invasion capacity of tumor plasma cells, but little is known about their role in the biology of MM CAF. In this study, we investigated the u-PA/u-PAR axis in MM-associated fibroblasts and explore additional mechanisms of tumor/stroma interplay in MM progression. METHODS: CAF were purified from total BM stromal fraction of 64 patients including monoclonal gammopathy of undetermined significance, asymptomatic and symptomatic MM, as well as MM in post-treatment remission. Flow cytometry, Real Time PCR and immunofluorescence were performed to investigate the u-PA/u-PAR system in relation to the level of activation of CAF at different stages of the disease. Moreover, proliferation and invasion assays coupled with silencing experiments were used to prove, at functional level, the function of u-PAR in CAF. RESULTS: We found higher activation level, along with increased expression of pro-invasive molecules, including u-PA, u-PAR and metalloproteinases, in CAF from patients with symptomatic MM compared to the others stages of the disease. Consistently, CAF from active MM as well as U266 cell line under the influence of medium conditioned by active MM CAF, display higher proliferative rate and invasion potential, which were significantly restrained by u-PAR gene expression inhibition. CONCLUSIONS: Our data suggest that the stimulation of u-PA/u-PAR system contributes to the activated phenotype and function of CAF during MM progression, providing a biological rationale for future targeted therapies against MM
Solution Structure of LC4 Transmembrane Segment of CCR5
CC-chemokine receptor 5 (CCR5) is a specific co-receptor allowing the entry of human immunodeficiency virus type 1 (HIV-1). The LC4 region in CCR5 is required for HIV-1 entry into the cells. In this study, the solution structure of LC4 in SDS micelles was elucidated by using standard 1H two-dimensional NMR spectroscopy, circular dichroism, and fluorescdence quenching. The LC4 structure adopts two helical structures, whereas the C-terminal part remains unstructured. The positions in which LC4 binds to the HIV-1 inhibitory peptide LC5 were determined by docking calculations in addition to NMR data. The poses showed the importance of the hydrophobic interface of the assembled structures. The solution structure of LC4 elucidated in the present work provides a structural basis for further studies on the HIV-1 inhibitory function of the LC4 region
Conformation and dynamics of biopharmaceuticals: Transition of mass spectrometry-based tools from academe to industry
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A Theoretical and Experimental Examination of Systematic Ligand-Induced Disorder in Au Dendrimer-Encapsulated Nanoparticles
In this paper we present a new methodology for the analysis of 1-2 nm nanoparticles using extended X-ray absorption fine structure (EXAFS) spectroscopy. Different numbers of thiols were introduced onto the surfaces of dendrimer-encapsulated Au nanoparticles, consisting of an average of 147 atoms, to systematically tune the nanoparticle disorder. An analogous system was investigated using density functional theory molecular dynamics (DFT-MD) simulations to produce theoretical EXAFS signals that could be directly compared to the experimental results. Validation of the theoretical results by comparing to experiment allows us to infer previously unknown details of structure and dynamics of the nanoparticles. Additionally, the structural information that is learned from theoretical studies can be compared with traditional EXAFS fitting results to identify and rationalize any errors in the experimental fit. This study demonstrates that DFT-MD simulations accurately depict complex experimental systems in which we have control over nanoparticle disorder, and shows the advantages of using a combined experimental/theoretical approach over standard EXAFS fitting methodologies for determining the structural parameters of metallic nanoparticles.Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U. S. Department of Energy DE-FG02-09ER16090Robert A. Welch Foundation F-0032Department of Energy DE-FG02-03ER15476U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences DE-AC02-98CH10886Synchrotron Catalysis Consortium, U. S. Department of Energy DE-FG02-05ER15688National Institute on Minority Health and Health Disparities from the National Institutes of Health G12MD007591Chemistr
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