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News & Events At The Texas Center For Superconductivity

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Bi-Weekly Seminar

Development of Nanostructured Systems for Energy, Environmental and Biomedical Applications

by: Karen Martirosyan

Date: Friday September 18, 2009

Time: 12:00 pm – 1:00 pm

Location: Houston Science Center – Building 593 — Room 102

Overview

The main topic of this presentation will focus on development of nanostructured particulate systems and fabrication of advanced devices for power systems, energy storage, environmental protection, national security and health care. I will present novel nanoenergetic systems that have the potential to enable a more concentrated energy release and potentially can be used for various military applications such as an actuation parts, igniter, propulsion unit, gas-generators as well as an active part for high power electromagnetic pulse generators. I will describe a novel cost-effective and energy efficient production of nanostructured complex oxides that we referred to as Carbon Combustion Synthesis of Oxides (CCSO). In this process, the reactive oxidation of carbon/graphite nanoparticles generates a steep thermal wave (temperature gradient of up to 500 °C/cm) that propagates through the solid reactant mixture (oxides, carbonates or nitrates) converting it to the desired products. The high rate of gas release enables synthesis of highly porous complex oxides having a particle size in the range of 50-800 nm. The experimental results of fabrication of various systems such as hard and soft magnetic materials, superconductors, multiferroics, bulk ceramic resistors, capacitors, photocatalysts with p-n junction, MRI contrast agents and cancer hyperthermia will be presented. Key factors that affected to the device characteristics (magnetization, conductivity, magnetic resonance relaxivity and other) will be discussed. Finally, I will describe a novel medical device that we referred to as Encapsulated Contrast Agent Marker (ECAM) for MRI cancer prostate brachytherapy (PB). While MRI is the modern superior imaging modality, for cancer treatment it is currently not used in PB because the implanted radioactive titanium seeds appear artifacts (negative contrast) and cannot be accurately localized within the prostate and periprostatic tissue. The innovative development of an MRI visible ECAMs technology will provide a precise targeted magnetic resonance imaging for PB and can impact over 200,000 in US (12,000 in Texas) men diagnosed annually with localized prostate cancer. Development of this emerging technologies warrant a multifaceted approach, which includes interdisciplinary collaboration, partnerships with industry and academia, and integration of modern problems into our curriculum.

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Bi-Weekly Seminar

Ion Implantation, Past, Present, and Future: The Future is in the Area of Material Modification for Biology Research

by: Prof. Wei-Kan Chu

Date: Friday September 04, 2009

Time: 12:00 pm – 1:00 pm

Location: Houston Science Center – Building 593 — Room 102

Overview

Ion Implantation is the injection of energetic ions into a solid, thereby changing the physical properties of the solid by impurity doping, and/or by radiation damage. It is mostly used in semiconductor device fabrication and in metal finishing as well as in various applications in materials science research and technology. In this talk, I will briefly review the process of ion implantation, its characteristics, and its applications in material modification. I will give a few examples of our current activities using ion implantation. More importantly, I will be proposing applications related to ion beam modification of soft materials for biological applications. Although ion implantation has been around for more than forty years, biological applications of ion implantation have come of age gradually in the last decade or so. I will be discussing some recent developments in ion implantation modification of polymers and ion beam modification of surface hydrophilicity for applications in protein pattern printing and subsequent living cell adhesion. The intention of this talk is to seek feedback, interaction, and collaboration from the biology, biochemistry, biophysics, and biomedical communities.

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Bi-Weekly Seminar

Electron Beam Characterization of YBa2Cu3O7-δ

by: Prof. James K. Meen

Date: Friday August 21, 2009

Time: 12:00 pm – 1:00 pm

Location: Houston Science Center – Building 593 — Room 102

Overview

There are significant challenges to characterizing YBa2Cu3O7-δ (Y123) by electron microbeam but the results obtained have considerable utility. Few samples of Y123 have that cation stoichiometry. Variations within individual monoliths are used to map crystallization sequence and it will be shown that this is not necessarily from a single nucleus. Melting relations under different partial pressures of oxygen are employed to show that copper is in mixed valence state in Y-Ba-Cu oxide liquids even in pure oxygen and this has its own influence on the phase relations and in crystallization of Y123. Determination of oxygen content of Y123 is critical in its characterization but is altered by procedures used to prepare samples for analysis and by aging of the samples. The Cu L self-absorption spectrum of Y123 shows marked changes with oxygen doping and varies within some samples on a micron-scale.

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Bi-Weekly Seminar

Electric Field Driven Torque in Rotary Biological Motors

by: Prof. John H. Miller

Date: Friday July 24, 2009

Time: 12:00 pm – 1:00 pm

Location: Houston Science Center – Building 593 — Room 102

Overview

Rotary motors, including ATP synthase, V-type ATPases, and the bacterial flagellar motor, play crucial roles in living organisms. In humans and other eukaryotes, ATP synthase operates in the inner membranes of mitochondria to produce adenosine triphosphate (ATP), life’s chemical currency of energy. V-type ATPases utilize the energy of ATP hydrolysis to create electrochemical potential differences (usually of protons) across diverse biological membranes. I will describe our recently proposed electric field driven torque model of ion-driven rotary motors. The model predicts a scaling law relating torque to the number of ion-carrying subunits in the rotor, the number of stators, and the ion motive force across the membrane. When the FO complex of ATP synthase is coupled to F1, the model predicts a minimum proton motive force (pmf) needed to drive ATP production by F1. By contrast the model predicts a maximum pmf against which the V1 complex of a V-type ATPase can overcome the opposing torque by V0 to pump protons back across the membrane. We are also working to develop label-free electromagnetic sensors to detect activity and possible dysfunction of mitochondrial and other enzymes. Dysfunction of mitochondrial enzymes has been implicated in type-2 diabetes, cancer, heart disease, and neurodegenerative diseases, while dysfunction of V-type ATPases has been implicated in osteopetrosis, distal renal tubular acidosis, and many other diseases. Therefore, improved understanding of such enzymes is broadly significant to human health.

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Bi-Weekly Seminar

Modulation of Calmodulin Plasticity by the Effect of Macromolecular Crowding

by: Margaret S. Cheung

Date: Friday May 22, 2009

Time: 12:00 pm – 1:00 pm

Location: Houston Science Center – Building 593 — Room 102

Overview

In vitro biochemical reactions are most often studied in dilute solution, a poor mimic of the intracellular space of eukaryotic cells which are crowded with mobile and immobile macromolecules. Such crowded conditions exert volume exclusion and other entropic forces that have the potential to impact chemical equilibria and reaction rates. In this article, we used the well characterized and ubiquitous molecule calmodulin (CaM) and a combination of theoretical and experimental approaches to address how crowding impacts CaM's conformational plasticity. CaM is a dumbbell shaped molecule that contains four EF hands (two in the N-lobe and two in the C-lobe) that each could bind Ca2+ leading to stabilization of certain substates that favor interactions with other target proteins. Using coarse-grained molecular simulations, we explored the distribution of CaM conformations in the presence of crowding agents. These predictions in which crowding effects enhances the population of compact structures were then confirmed in experimental measurements using fuorescence resonance energy transfer techniques of donor/acceptor labeled CaM under normal and crowded conditions. We further explored the folding energy landscape and examined the structural characteristics of CaM at free energy basins using protein reconstruction methods. We discovered that crowding stabilizes several different compact conformations, which refects the inherent plasticity in CaM's structure. From these results, we suggest that the EF hands in the C-lobe are fexible and can be thought of as a switch, while those in the N-lobe are stiff as analogous to a rheostat. New combinatorial signaling properties may arise from the product of the differential plasticity of the two distinct lobes of CaM in the presence of crowding. We discuss the implications of these results for modulating CaM's ability to bind Ca2+ and target proteins.

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