Application and correlation of nano resolution microscopy techniques to viral protein localization

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Title Application and correlation of nano resolution microscopy techniques to viral protein localization
Publication Type dissertation
School or College College of Science
Department Physics & Astronomy
Author Hodges, Jeffery Allen
Date 2013-12
Description This dissertation is primarily focused on the application of superresolution microscopy techniques to localization of viral proteins within envelope viruses. Advances in optical super-resolution microscopy techniques have enabled scientists to observe phenomena much smaller than the Abbe diffraction limit by stochastically limiting the number of molecules excited at a given instance and localizing their positions one at a time. Additionally, methods such as Atomic Force Microscopy (AFM) allow scientists to measure the topological features and material properties of samples through contact with a force probe. This dissertation describes the application of these two techniques to virology in order to localize internal viral proteins of enveloped virions, and measure their effect on the elastic properties of the virion. By utilizing super-resolution microscopy techniques such as Fluorescent Photo-Activated Localization Microscopy (fPALM) on virions, which have had their surface glycoproteins labeled with a photo-switchable label, the viral envelope may be accurately recovered. This dissertation describes the development and application of this technique as it applies to envelope recovery of Vesicular Stomatitis Virus (VSV) and Human Immunodeficiency Virus-1 (HIV-1). By fluorescently labeling proteins, which are internal to each of these viruses, I have been able to localize a variety of viral proteins within their recovered envelopes. This is done without significant damage to the virion, making this method a highly effective in vivo technique. In the case of VSV, an asymmetric localization along the central axis towards the blunt 5' end was found to exist for both the polymerase and phosphoproteins. These have been determined to occupy a region in the central cavity of ~57 +/-12 nm on the 5' end. This inhomogeneity of the underlying proteins such an asymmetry would predict that the Young's modulus would vary along the central axis of the virion. This dissertation also describes utilizing AFM to explore and measure the variance in young's modulus between the two distinct elastic regions observed in VSV virions, which vary by 12% in elasticity. From these combined results I have found a strong correlation between the two methodologies in order to calculate the distribution of polymerases within VSV.
Type Text
Publisher University of Utah
Subject Atomic force microscopy; Biomaterials; Nano optics; PALM; STORM; Vesicular stomatitis virus
Dissertation Name Doctor of Philosophy
Language eng
Rights Management Copyright © Jeffery Allen Hodges 2013
Format application/pdf
Format Medium application/pdf
Format Extent 1,980,659 bytes
Identifier etd3/id/2681
ARK ark:/87278/s6ck1nnj
Setname ir_etd
ID 196256
Reference URL https://collections.lib.utah.edu/ark:/87278/s6ck1nnj
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