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Yes / A novel beam-forming module based on Wilkinson power divider technology, including attenuators and phase shifter chips is designed, fabricated and evaluated to be incorporated in a Relay Station connecting it with the Base Station under a 4G network. The proposed module is a 1:8 port circuit, utilizing two substrates, providing approximately 700 MHz bandwidth over 3.5 GHz frequency band and less than −20 dB transmission line coupling. Moreover an external control unit that feeds the beam-forming module with code-words that define the proper amplitude/phase of the excitation currents is established and described. The presented module is connected to a planar array and tested for two beam-forming scenarios, providing satisfactory radiation patterns.

Cytolysin A (ClyA) is a member of a class of proteins called pore-forming toxins (PFTs). ClyA is secreted by Gram-negative bacteria, and it attacks a number of mammalian cells by inserting into and forming channels within the cell membrane (Oscarsson J et al., 1999). It has been suggested that ClyA binds to cholesterol (Oscarsson J et al., 1999) and thus can insert into the membranes of many different cell types of eukaryotic origin. In our studies we propose to engineer a ClyA protein that can only attack a small subset of cell types. We propose to engineer ClyA that can be only activated when exposed to specific cell-surface proteases produced by a specific cell type. We ultimately want to target breast cancer cells that differentially secrete or express proteases such as matrix-metalloproteases (Stautz D et al., 2012; Zhang, M et al. 2013). To engineer this protein we took advantage of the N-terminus of ClyA. The N-terminus of ClyA, which is highly hydrophobic (Oscarsson J et al), undergoes a conformational change to insert into the target cell membrane (Oscarsson J et al). This conformational change allows ClyA to penetrate the target membrane to form a transmembrane domain of ClyA. The hydrophobic nature of lipid membranes makes it highly unfavorable for any charged residues to cross the membrane (Hunt J 1997). With this in mind, we hypothesize that negative charges inserted into the N-terminus of ClyA will inhibit it from inserting into the membrane. Thus, we mutated the N-terminus of the ClyA protein by inserting an inactivation site composed of negatively charged amino acids that we hypothesize would prevent insertion into the plasma membrane of the target cell. Once we confirmed that this construct was an inactive ClyA mutant, we inserted a thrombin cleavage site right after the inserted negative charges. This site should allow us to remove the negative charges once the protein is exposed to thrombin. Once the negative charges are removed, the protein should recover its activity. This approach will allow us to create a version of ClyA that is protease-switchable.

Porous ceramics have successfully been used in a wide variety of highly advanced applications. Current routes to porous ceramics are limited in the types of porosity they can create and no one process is flexible enough to create any desired structure. This study introduces the use of ice particles as pore forming agents to fabricate porous materials. This novel method possesses several advantages over current industrial techniques including environmental friendliness, low cost, and flexibility in size and shape of resulting pores. Porous ceramic structures were created by adding preformed ice particles to an alumina slurry which was quickly frozen, air dried, and then sintered. Porosity was characterized using Scanning Electron Microscopy (SEM), Archimedes measurements, and gas sorption techniques. Small spherical pores were successfully created in the 20-200?m range and larger spherical pores were also created in the 2-3 mm range. Amount of porosity was controlled through specifying the amount of ice added to the ceramic slurry. Samples were prepared with porosity levels ranging from 30-75%. As a completely new process, these initial results are quite promising and further development will allow for even greater morphology control. / Master of Science

Brucella causes undulant fever in humans and uterine and systemic infection leading to abortions in domestic animals and wild life. For the acquisition of iron in mammalian hosts, species of Brucella are known to produce two siderophores, 2, 3-dihydroxy benzoic acid (2, 3-DHBA) and brucebactin. Inability to synthesize of 2, 3-DHBA affects the ability of pathogen to metabolize erythritol, replicate in trophoblast cells and cause abortion in pregnant ruminant host. The entF gene has been implicated in the unresolved pathway allowing brucebactin biosynthesis in Brucella. The research effort presented in this thesis tries to relate the role of entF in iron acquisition and potential relation with erythritol metabolism by wild type B. abortus 2308. An entF deletion mutant (BAN1) of B. abortus 2308, generated using cre-lox methodology was found to be growth inhibited in iron minimal media compared to wild type strain. Growth inhibition was further enhanced with the addition of an iron chelator or 0.1% erythritol. Compared to wild type strain, no growth inhibition of BAN1 mutant was found in murine J774A.1 macrophages, which suggests that Brucella could acquire iron inside mammalian cells. The entF gene complemented mutant strains of BAN1 (BAN2A and BAN2B) were found to be intermediate in their ability to grow in iron minimal media supplemented with 0.0.05% erythritol, when compared to wild type and BAN1 strain. The results from the present thesis demonstrate that entF gene plays an important role in iron acquisition and erythritol metabolism by B. abortus 2308 under iron limiting conditions. / Master of Science

Collagen type I is an extracellular matrix (ECM) protein that affords tensile strength and biological scaffolding to numerous vertebrate and invertebrate tissues. This strength has been attributed to the triple-helical structure of the collagen type I molecules, their organization into fibrils, and the presence of inter-molecular, covalent, enzymatic crosslinks. There are several different types of these crosslinks; their composition is tissue-specific and dependent upon factors such as age and health. Furthermore, these enzymatic crosslinks tend to form specifically at amino/N- and carboxy/C-terminal crosslinking sites. The mechanical behavior of collagen type I has been investigated, via experiment and theory, at the level of the molecule, microfibril, fibril, and fiber. However, the influence of different enzymatic crosslinks and their location (e.g., N- vs. C-site) on the mechanics of collagen type I has not been investigated in the literature. We employed molecular dynamics to model the mechanical behavior of uncrosslinked and crosslinked ~23-nm-long molecular segments and ~65-nm-long microfibril units of collagen type I. We then used these molecular simulations to construct a model of a single collagen type I fibril by considering the ~65-nm-long microfibril units arranged in series and then in parallel. When a uniaxial deformation was applied along the long axis of the molecular models, N-crosslinks aligned rapidly at lower strains followed by C-crosslinks more gradually at higher strains, leading to a two-stage crosslink recruitment. Then when comparing the influence of different enzymatic crosslinks, significant differences were observed for the high-strain elastic moduli of our microfibril unit models, namely and in increasing order, uncrosslinked, immature crosslinked (HLKNL and deH-HLNL), mature HHL-crosslinked, and mature PYD-crosslinked. At the fibril level, our low- and high-strain elastic moduli were in good agreement with some literature data, but in over-estimation of several other literature reports. Future work will seek to address simplifications and limitations in our modeling approach. A model such as this, accounting for different enzymatic crosslink types, may allow for the prediction of the mechanics of collagen fibrils and collagenous tissues, in representation of healthy and diseased states. / Ph. D.

Yes / In the study of microbial keratitis, in vivo animal models often require a large number of animals, and in vitro monolayer cell culture does not maintain the three-dimensional structure of the tissues or cell-to-cell communication of in vivo models. Here, we propose reproducible ex vivo models of single- and dual-infection keratitis as an alternative to in vivo and in vitro models. / Wellcome Trust

O tratamento superficial de shot peening tem por objetivo aumentar a resistência à fadiga sendo comparada pelas medidas de tensão residual. O processo peen forming é uma variante do processo shot peening onde se obtém uma curvatura na placa produzida pelo jateamento das esferas através da compressão dos grãos localizados próximos à superfície. Foi estudado neste trabalho a influência dos parâmetros pressão e tamanho de granalha, utilizado no processo de peen forming, no perfil de tensão residual e no raio de curvatura em amostras de alumínio 7050. A avaliação do perfil de tensão de residual foi efetuada por difração de raios-x utilizando o método de sen2 . Os resultados mostram que a formação da altura do arco de curvatura é proporcional a pressão de jateamento e ao tamanho das esferas e inversamente proporcional a espessura da amostra, e que o fator de concentração de tensões é maior para amostras jateadas com menores esferas. Na seção final deste trabalho apresenta um estudo complementar sobre microdeformação e tamanho médio de cristalito, podendo avaliar o perfil das amostras após jateamento. / Shot peening is a superficial cold work process used to increase the fatigue life evaluated by residual stress measurements. The peen forming process is a variant of the shot peening process, where a curvature in the plate is obtained by the compression of the grains near to the surface. In this paper, the influence of the parameters such as: pressure of shot, ball shot size and thickness of aluminum 7050 samples with respect to residual stress profile and resulting arc height was studied. The evaluation of the residual stress profile was obtained by sin2 method. The results show that the formation of the curvature arc height is proportional to the shot peening pressure, of spheres size and inversely proportional to the thickness of the sample, and that stress concentration factor is larger for samples shot peened with small balls. On final of this paper presents an additional study on microstrain and average crystallite size, which can evaluate the profile of the samples after blasting.