Ricostruzione degli sforzi in elementi finiti di piastra

Nell’ambito dell’analisi computazionale delle strutture il metodo degli elementi finiti è probabilmente uno dei metodi numerici più efficaci ed impiegati. La semplicità dell’idea di base del metodo e la relativa facilità con cui può essere implementato in codici di calcolo hanno reso possibile l’applicazione di questa tecnica computazionale in diversi settori, non solo dell’ingegneria strutturale, ma in generale della matematica applicata. Ma, nonostante il livello raggiunto dalle tecnologie ad elementi finiti sia già abbastanza elevato, per alcune applicazioni tipiche dell’ingegneria strutturale (problemi bidimensionali, analisi di lastre inflesse) le prestazioni fornite dagli elementi usualmente utilizzati, ovvero gli elementi di tipo compatibile, sono in effetti poco soddisfacenti. Vengono in aiuto perciò gli elementi finiti basati su formulazioni miste che da un lato presentano una più complessa formulazione, ma dall’altro consentono di prevenire alcuni problemi ricorrenti quali per esempio il fenomeno dello shear locking. Indipendentemente dai tipi di elementi finiti utilizzati, le quantità di interesse nell’ambito dell’ingegneria non sono gli spostamenti ma gli sforzi o più in generale le quantità derivate dagli spostamenti. Mentre i primi sono molto accurati, i secondi risultano discontinui e di qualità scadente. A valle di un calcolo FEM, negli ultimi anni, hanno preso piede procedure di post-processing in grado, partendo dalla soluzione agli elementi finiti, di ricostruire lo sforzo all’interno di patch di elementi rendendo quest’ultimo più accurato. Tali procedure prendono il nome di Procedure di Ricostruzione (Recovery Based Approaches). Le procedure di ricostruzione qui utilizzate risultano essere la REP (Recovery by Equilibrium in Patches) e la RCP (Recovery by Compatibility in Patches). L’obbiettivo che ci si prefigge in questo lavoro è quello di applicare le procedure di ricostruzione ad un esempio di piastra, discretizzato con vari tipi di elementi finiti, mettendone in luce i vantaggi in termini di migliore accurattezza e di maggiore convergenza.

Interazioni tra le glicoproteine D, B, H ed L critiche per la fusione indotta dal virus Herpes simplex

Four glycoproteins (gD, gB, gH, and gL) are required for herpes simplex virus (HSV) entry into the cell and for cell-cell fusion in transfected cells. gD serves as the receptor-binding glycoprotein and as the trigger of fusion; the other three glycoproteins execute fusion between the viral envelope and the plasma or endocytic membranes. Little is known on the interaction of gD with gB, gH, and gL. Here, the interactions between herpes simplex virus gD and its nectin1 receptor or between gD, gB, and gH were analyzed by complementation of the N and C portions of split enhanced green fluorescent protein (EGFP) fused to the glycoproteins. Split EGFP complementation was detected between proteins designated gDN + gHC, gDN + gBC, and gHN + gBC + wtgD, both in cells transfected with two or tree glycoproteins and in cells transfected with the four glycoproteins, commited to form syncytia. The in situ assay provides evidence that gD interacts with gH and gB independently one of the other. We further document the interaction between gH and gB. To elucidate which portions of the glycoproteins interact with each other we generated mutants of gD and gB. gD triggers fusion through a specialised domain, named pro-fusion domain (PFD), located C-terminally in the ectodomain. Here, we show that PFD is made of subdomains 1 and 2 (amino acids 260–285 and 285–310) and that each one partially contributed to herpes simplex virus infectivity. Chimeric gB molecules composed of HSV and human herpesvirus 8 (HHV8) sequences failed to reach the cell surface and to complement a gB defective virus. By means of pull down experiments we analyzed the interactions of HSV-HHV8 gB chimeras with gH or gD fused to the strep-tag. The gB sequence between aa residues 219-360 was identified as putative region of interaction with gH or critical to the interaction.

Variazione dei markers di attivata coagulazione indotta dalla terapia infusionale con Infliximab in pazienti affetti da malattie infiammatorie croniche intestinali

INTRODUCTION: A relationship between inflammatory response and coagulation is suggested by many observations. In particular, pro-inflammatory cytokines, such as TNFalpha, promote the activation of coagulation and reduce the production of anticoagulant molecules. It is known that inflammatory bowel diseases show a prothrombotic state and a condition of hypercoagulability. Aim of our study was to evaluate whether anti-TNFalpha therapy induces changes in the levels of coagulation activation markers in IBD patients. MATERIALS AND METHODS: We analyzed 48 plasma samples obtained before and 1 hour after 24 infliximab infusions (5 mg/kg) in 9 IBD patients (5 men and 4 women; mean age: 47.6+17.6 years; 4 Crohn's disease, 4 Ulcerative Colitis,1 Indeterminate Colitis). F1+2 and D-dymer levels were measured in each sample using ELISA methods.The data were statistically analyzed by means of Wilcoxon matched paired test. RESULTS: Median F1+2 levels were markdely reduced 1 hour after anti-TNFα infusion (median pre-infusion levels were 247.0 pmol/L and median post-infusion levels were 185.3 pmol/L) (p<0.002). Median D-dymer levels were also significantly reduced, from 485.2 ng/mL to 427.6 ng/mL (p< 0.001). These modifications were more evident in patients naive for infliximab therapy (p<0.02 for F1+2 and p<0.02 for D-dymer) and in Crohn's disease compared with Ulcerative Colitis patients (p=0.01 for F1+2 and p<0.007 for D-dymer).CONCLUSIONS: Infusion of infliximab significantly reduces the activation of coagulation cascade in IBD patients. This effect is early enough to suggest a direct effect of infliximab on the coagulation cascade and a possible new anti-inflammatory mechanism of action of this molecule.

Paralelización de un algoritmo de ray tracing para arrays de mililentes

Máster Universitario en Sistemas Inteligentes y Aplicaciones Numéricas en Ingeniería (SIANI)