Barrett, The Honors College at Arizona State University proudly showcases the work of undergraduate honors students by sharing this collection exclusively with the ASU community.

Barrett accepts high performing, academically engaged undergraduate students and works with them in collaboration with all of the other academic units at Arizona State University. All Barrett students complete a thesis or creative project which is an opportunity to explore an intellectual interest and produce an original piece of scholarly research. The thesis or creative project is supervised and defended in front of a faculty committee. Students are able to engage with professors who are nationally recognized in their fields and committed to working with honors students. Completing a Barrett thesis or creative project is an opportunity for undergraduate honors students to contribute to the ASU academic community in a meaningful way.

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Description

Single molecule FRET experiments are important for studying processes that happen on the molecular scale. By using pulsed illumination and collecting single photons, it is possible to use information gained from the fluorescence lifetime of the chromophores in the FRET pair to gain more accurate estimates of the underlying FRET

Single molecule FRET experiments are important for studying processes that happen on the molecular scale. By using pulsed illumination and collecting single photons, it is possible to use information gained from the fluorescence lifetime of the chromophores in the FRET pair to gain more accurate estimates of the underlying FRET rate which is used to determine information about the distance between the chromophores of the FRET pair. In this paper, we outline a method that utilizes Bayesian inference to learn parameter values for a model informed by the physics of a immobilized single-molecule FRET experiment. This method is unique in that it combines a rigorous look at the photophysics of the FRET pair and a nonparametric treatment of the molecular conformational statespace, allowing the method to learn not just relevant photophysical rates (such as relaxation rates and FRET rates), but also the number of molecular conformational states.

ContributorsSafar, Matthew Matej (Author) / Presse, Steve (Thesis director) / Sgouralis, Ioannis (Committee member) / Department of Physics (Contributor) / School of Mathematical and Statistical Sciences (Contributor, Contributor) / Barrett, The Honors College (Contributor)
Created2021-05
Description
Diffusion coefficients often vary across regions, such as cellular membranes, and quantifying their variation can provide valuable insight into local membrane properties such as composition and stiffness. Toward quantifying diffusion coefficient spatial maps and uncertainties from particle tracks, we use a Bayesian method and place Gaussian Process (GP) Priors on

Diffusion coefficients often vary across regions, such as cellular membranes, and quantifying their variation can provide valuable insight into local membrane properties such as composition and stiffness. Toward quantifying diffusion coefficient spatial maps and uncertainties from particle tracks, we use a Bayesian method and place Gaussian Process (GP) Priors on the maps. For the sake of computational efficiency, we leverage inducing point methods on GPs arising from the mathematical structure of the data giving rise to non-conjugate likelihood-prior pairs. We analyze both synthetic data, where ground truth is known, as well as data drawn from live-cell single-molecule imaging of membrane proteins. The resulting tool provides an unsupervised method to rigorously map diffusion coefficients continuously across membranes without data binning.
ContributorsKumar, Vishesh (Author) / Presse, Steve (Thesis director) / Bryan IV, J. Shep (Committee member) / Barrett, The Honors College (Contributor) / School of Mathematical and Statistical Sciences (Contributor) / Department of Physics (Contributor)
Created2024-05
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Description

Bdellovibrio bacteriovorus (BB) is a gram negative predatory bacteria that uses other gram negative bacteria to proliferate non-binarily. Due to the predatory nature of BB researchers have proposed to use it as a potential biocontrol agent against other gram negative bacteria. The in vivo effect of predatory bacteria on a

Bdellovibrio bacteriovorus (BB) is a gram negative predatory bacteria that uses other gram negative bacteria to proliferate non-binarily. Due to the predatory nature of BB researchers have proposed to use it as a potential biocontrol agent against other gram negative bacteria. The in vivo effect of predatory bacteria on a living host lacks thorough investigation. This paper explores BB inside and outside of the C. elegans. BB acts internally by pre- infecting C. elegans with E. coli and then treating the worms with BB. After BB treatment worm survivavbility increased and morbidity decreased. Ex- ternally, BB modulated the environment around the nematode which reduced infection rates and increased nematode lifespan and survivability. Together, the internal and external results suggest BB has the capability to act as a living antibiotic acting topically and internally to reduce infection rates.

ContributorsStambolic, Milena (Author) / Presse, Steve (Thesis director) / Vlcek, Jessi (Committee member) / Barrett, The Honors College (Contributor) / Department of Physics (Contributor) / School of Mathematical and Statistical Sciences (Contributor)
Created2022-05
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Description

Electron Multiplying Charge Coupled Device (EMCCD) cameras are widely used for fluorescence microscopy experiments. However, the quantitative determination of biological parameters uniquely depends on characteristics of the unavoidably inhomogenous illumination profile as it gives rise to an image. It is therefore of interest to learn this inhomogenous illumination profiles that

Electron Multiplying Charge Coupled Device (EMCCD) cameras are widely used for fluorescence microscopy experiments. However, the quantitative determination of biological parameters uniquely depends on characteristics of the unavoidably inhomogenous illumination profile as it gives rise to an image. It is therefore of interest to learn this inhomogenous illumination profiles that can dramatically vary across images alongside the camera parameters though a detailed camera model. In this manuscript we create a detailed model to learn inhomogeneous illumination profiles as well as learn all associated camera parameters. We achieve this within a Bayesian paradigm allowing us to determine full distributions over the unknowns.

ContributorsBryan, Eric (Author) / Presse, Steve (Thesis director) / Fazel, Mohammed (Committee member) / Barrett, The Honors College (Contributor) / School of Mathematical and Statistical Sciences (Contributor) / Department of Physics (Contributor)
Created2022-05