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Applications of synchrotron radiation Laue diffraction in molecular structure studiesMaginn, Stephen James January 1989 (has links)
No description available.
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A neutron reflectivity study of thin filmsHarwood, N. M. January 1987 (has links)
No description available.
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Trapped-Mg+ Apparatus for Control and Structure StudiesToppozini, Laura 11 1900 (has links)
<p> Trapped ions can be isolated from external perturbations such as collisions with other atoms or electric and magnetic field inhomogeneities. For this reason, trapped ions can be useful in spectral measurements, quantum information technology and studying quantum behaviour. In this thesis, I discuss a trapped-Mg+ apparatus for studying the quantum mechanics of atoms. I describe the laser interactions that allow us to coherently excite our atoms. I go on to discuss the actual apparatus for trapping ions and making precise measurements, the hyperfine structure of 25 Mg+ and a proposed linewidth measurement. </p> / Thesis / Master of Science (MSc)
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Molecular Mechanism of E. coli ATP synthase: Structural Analysis of the Proton Channel2013 April 1900 (has links)
Adenosine triphosphate (ATP) is the energy currency of all living cells and its production is a key reaction in the energy metabolism of living organisms. Cells produce most of the ATP they require through ATP synthase, a unique molecular rotary motor driven by the movement of protons across the lipid membrane. In E.coli, ATP synthase is composed of a soluble domain called F1, which houses the catalytic sites, and a transmembrane domain called F0 that shuttles protons across the membrane to drive ATP production in the F1 sector. The F0 domain is built of three subunit types: subunit a and a dimer of subunit b form the stator of the motor, while a decameric c ring forms the rotor. The dynamic interface between a and c10 forms the proton channel. The ultimate goal of this work is to determine the structure of the proton transport machinery and understand the molecular mechanism of proton translocation in ATP synthase. We have characterized some of the key events in the stepwise assembly of the F0--complex. We have designed and validated a model protein, consisting of genetically fused subunits a and c, for structural studies. We have made progress towards determining the structure of the proton channel, including the development of a novel procedure for purification of subunit a and the a/c fusion protein, and crystallization of subunit a. Medical applications of this work include the potential development of novel antibiotic compounds, as well as the characterization and potential treatment of three human diseases caused by disruptions in proton transport through F0.
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