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  <title><![CDATA[MS Defense by Jessica Pfliger]]></title>
  <body><![CDATA[<p>In partial fulfillment of the requirements for the degree of</p>

<p>&nbsp;</p>

<p>Master of Science in Biology</p>

<p>in the</p>

<p>School of Biological Sciences</p>

<p>&nbsp;</p>

<p><strong>Jessica Pfliger</strong></p>

<p>&nbsp;</p>

<p>Will defend her thesis</p>

<p>&nbsp;</p>

<p><strong>&ldquo;CHARACTERIZATION OF A CHROMATINIZED HYDROGEN PEROXIDE BIOSENSOR IN CANCER CELLS&rdquo;</strong></p>

<p>&nbsp;</p>

<p><strong>14, February 2022</strong></p>

<p>&nbsp;1:00pm</p>

<p><a href="https://bluejeans.com/126058378">https://bluejeans.com/126058378</a></p>

<p>&nbsp;</p>

<p>&nbsp;</p>

<p><strong>Thesis Advisor:</strong></p>

<p>Dr. Yuhong Fan</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p>&nbsp;</p>

<p><strong>Committee Members:</strong></p>

<p>Dr. Alfred Merrill</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p>&nbsp;</p>

<p>&nbsp;Dr. Hengbin Wang</p>

<p>Department of Biochemistry and Molecular Genetics</p>

<p>School of Medicine</p>

<p>University of Alabama at Birmingham</p>

<p>&nbsp;&nbsp;</p>

<p><strong>Abstract: </strong></p>

<p>Hydrogen Peroxide (H<sub>2</sub>O<sub>2</sub>) is an important eukaryotic signaling molecule regulating cellular processes. As one of the most abundant reactive oxidative species (ROS), H<sub>2</sub>O<sub>2</sub> can cause oxidative stress and cytotoxicity at elevated concentrations leading to DNA damage and programmed cell death. Despite the recent advancements in modulating ROS responses for potential cancer therapies, little is known about nuclear ROS temporal emergence and dynamics. To investigate the role of nuclear ROS and H<sub>2</sub>O<sub>2</sub> in chromatin, we established a genetically engineered chromatin-targeted biosensor for H<sub>2</sub>O<sub>2</sub>, H2B-HyPer, by fusion of HyPer, a specific H<sub>2</sub>O<sub>2</sub> biosensor, with core histone H2B. In this thesis, I utilized fluorescent microscopy and fluorescent recovery after photobleaching (FRAP) to study the H<sub>2</sub>O<sub>2</sub> dynamics within the chromatin of HCT116 colon cancer cells containing genetically integrated H2B-HyPer. I demonstrate that H2B-HyPer is localized in the nucleus of HCT116/H2B-HyPer cells with an average residence time and mobile fraction of 9.14 minutes and 20.59%, respectively, comparable to the core histones in chromatin. I then show that H2B-HyPer is sensitive to changes in H<sub>2</sub>O<sub>2</sub> levels post addition of H<sub>2</sub>O<sub>2</sub> or DTT in culture medium. Further analysis of H2B-HyPer kinetics revealed a rapid increase and recovery of H2B-HyPer signal intensity in HCT116/H2B-HyPer cells upon treatment with and the removal of H<sub>2</sub>O<sub>2</sub>. Altogether, these studies establish H2B-HyPer as an effective biosensor for real-time spatio-temporal tracking of chromatin-proximal H<sub>2</sub>O<sub>2</sub> dynamics.</p>
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