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  <title><![CDATA[PhD Proposal by Zhou Yuan]]></title>
  <body><![CDATA[<p>BioE PhD Proposal Presentation- Zhou Yuan</p>

<p><strong>&nbsp;</strong></p>

<p><strong>Zhou Yuan</strong></p>

<p>Ph. D Proposal Presentation</p>

<p>Wednesday, January 18<sup>th</sup>, 2017, 3pm</p>

<p>3:00pm, IBB Seminar Room 1128</p>

<p><strong>&nbsp;</strong></p>

<p><strong>Advisor:</strong></p>

<p>Dr. Zhu (Georgia Institute of Technology)</p>

<p>&nbsp;</p>

<p><strong>Committee:</strong></p>

<p>Dr. Susan Thomas (Georgia Institute of Technology)</p>

<p>Dr.&nbsp;Michelle Krogsgaard (New York University)</p>

<p>Dr.&nbsp;Mandy Ford (Emory University)</p>

<p>Dr. Gabe Kwong (Georgia Institute of Technology)</p>

<p><strong>&nbsp;</strong></p>

<p><strong>&nbsp;</strong></p>

<p><strong>&nbsp;</strong></p>

<p><strong>Understanding the effect of tumor microenvironment on T cell antigen recognition</strong></p>

<p><strong>&nbsp;</strong></p>

<p>Skin cancer is the most common cancer in the United States, among which melanoma is the most serious type with high mortality rate. Despite the critical role of CD8<sup>+</sup> T cells in tumor clearance, their functions in the tumor microenvironment (TME) are impaired by immunosuppressive cells/cytokines, inhibitory receptors, and metabolic restriction. Targeting these pathways were shown to promote tumor clearance, yet unknown mechanisms may still exist curtailing the T cell responses. T cell activation has been shown to be largely determined by the <em>in situ</em> mechanokinetic properties of the binding of T cell receptor (TCR) to peptide-major histocompatibility complex (pMHC), which are sensitive to perturbations of the cellular environment. Our preliminary studies have shown that the molecular interactions involved in T cell antigen recognition are altered in the TME.<strong> The present thesis will study the extent of this alteration, how such alteration consequentially suppresses T cell effector functions, and what the underlying mechanisms are</strong>. This study aims to address these questions with animal models, highly-sensitive biomechanical assays of single molecules, and other cellular and bimolecular approaches. The outcome will greatly enhance our understanding of the impaired anti-tumor T cell responses and inspire novel strategies for cancer immunotherapy.</p>
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