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  <title><![CDATA[PhD Proposal by Anirudh Sivakumar]]></title>
  <body><![CDATA[<p>Anirudh Sivakumar<br />
BME PhD Proposal Presentation<br />
<br />
<strong>Date</strong>:2022-02-07<br />
<strong>Time</strong>: 2:00 PM<br />
<strong>Location / Meeting Link</strong>: IBB Suddath Seminar Room 1128 / Virtual Link: <a href="https://bluejeans.com/518957531/4900">https://bluejeans.com/518957531/4900</a><br />
<br />
<strong>Committee Members:</strong><br />
Gabe Kwong, PhD (Advisor), M.G. Finn, PhD, Peng Qiu, PhD, Erik Dreaden, PhD, John Blazeck, PhD<br />
<br />
<br />
<strong>Title</strong>: Logic-gated activity sensors for programmable cancer diagnostics<br />
<br />
<strong>Abstract</strong>: Advances in synthetic biology are playing a fundamental role in shaping the future of cancer diagnostics toward disease detection and treatment monitoring with higher precision. For example, in engineered T cells, sense-and-respond components that employ AND, OR, or NOT gates have been demonstrated for multiplexed and logical control of T cell responses to increase specificity of tumor-antigen recognition. These advances highlight the promise of synthetic biology for cancer applications, yet the vast majority of these strategies rely on genetic circuits and non-endogenous components, which are complex and may raise safety and immunogenicity concerns for regulatory approval. Therefore, there are outstanding opportunities to apply cell- and gene-free sensors that implement concepts from synthetic biology toward cancer applications. The objective of this thesis proposal is to develop AND-gated protease sensors that integrate design principles from synthetic biology for programmable immune sensing. Protease dysregulation underpins the hallmarks of cancer and immunity and has driven the development of activity-based nanosensors, a class of cell- and gene-free sensors that are administered systemically to query sites of disease and release a reporter upon proteolysis that can be detected in urine. Building on this work, this proposal will design and validate AND-gated activity sensors consisting of nanoparticles conjugated with cyclic peptides that release a reporter only in the presence of protease pairs by implementing AND gate logic. This concept will be tested in the context of anti-tumor T cell immunity. Secretion of proteases called granzymes is fundamental to T cell cytotoxicity but not specific to anti-tumor responses. Therefore, AND-gated sensing of granzymes and cancer-associated matrix metalloproteinases (MMPs) &ndash; which are implicated in several fundamental tumor processes &ndash; may increase selectivity for detection of anti-tumor immune activity. This proposal will design cyclic peptides that perform AND-gated sensing of granzymes and MMPs (Aim 1), develop mathematical models to predict design parameters that affect specificity (Aim 2), and evaluate urinary biomarkers produced by AND-gated sensors for noninvasive detection of anti-tumor responses to immune checkpoint blockade therapy (Aim 3). This proposal will lay the groundwork for the future design of cell- and gene-free sensors for logic-based cancer diagnostics.</p>

<p>&nbsp;</p>
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