Office of Undergraduate Research

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Emphasizing equitable and inclusive access to research opportunities, the University of Maryland's Office of Undergraduate Research (OUR) empowers undergraduates and faculty to engage and succeed in inquiry, creative activity, and scholarship. This collection includes materials shared by undergraduate researchers during OUR events. It also encompasses materials from Undergraduate Research Day 2020, Undergraduate Research Day 2021, and Undergraduate Research Day 2022, which were organized by the Maryland Center for Undergraduate Research.

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Author: search.filters.author.Meyer, Jonathon

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    Optimization of an in-house bacterial cell-free expression system to evaluate the design of toehold switch sensors for selected cervical precancer miRNA biomarkers
    (2024-07-19) Meyer, Jonathon; Zeidan, Quira; Spirito, Catherine
    Cervical cancer is a significant health burden for women across the globe. However, over 94% of all cervical deaths occured in low and middle income countries (LMICs) in 2022 alone. This reflects a broader trend of a lack of access to quality treatment options for cervical cancer due to socioeconomic barriers including limited trained professionals, financial resources, and access to proper screening. We are partnering with UMaryland iGEM, an undergradutate-led synthetic biology research team, to assist in the development of a low-cost, point-of-care screening device for detecting commonly upregulated miRNAs in cervical precancer patients to address this issue. The functionality of this device relies on a cell-free expression kit, referred to as a lysate, in order to properly transcribe the desired toehold switches in the paper-based assay and translate the fluorescent protein output. However, common commercial cell-free lysates are expensive which increases the cost of producing our device – ultimately hindering its accessibility in LMICs. To address this problem, we propose a method for producing and optimizing our own in-house cell-free lysate. In our method, we compare three lysates – commercially available myTXTL, a lysate developed by the Aberdeen Proving Ground, and our own lysate – using varying ratios of energy mix, lysate, and T7p14 deGFP HP plasmid to evaluate the ideal composition of these components for a cell-free expression kit. We quantify these relationships using fluorescence in order to determine the efficacy of our lysate and the ideal ratio of components for a cell-free, paper-based assay.
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    Optimization of an in-house bacterial cell-free expression system to evaluate the design of toehold switch sensors for selected cervical precancer miRNA biomarkers
    (2024-07-17) Meyer, Jonathon; Zeidan, Quira; Spirito, Catherine
    Cervical cancer is a significant health burden for women across the globe. However, over 94% of all cervical deaths occured in low and middle income countries (LMICs) in 2022 alone. This reflects a broader trend of a lack of access to quality treatment options for cervical cancer due to socioeconomic barriers including limited trained professionals, financial resources, and access to proper screening. We are partnering with UMaryland iGEM, an undergradutate-led synthetic biology research team, to assist in the development of a low-cost, point-of-care screening device for detecting commonly upregulated miRNAs in cervical precancer patients to address this issue. The functionality of this device relies on a cell-free expression kit, referred to as a lysate, in order to properly transcribe the desired toehold switches in the paper-based assay and translate the fluorescent protein output. However, common commercial cell-free lysates are expensive which increases the cost of producing our device – ultimately hindering its accessibility in LMICs. To address this problem, we propose a method for producing and optimizing our own in-house cell-free lysate. In our method, we compare three lysates – commercially available myTXTL, a lysate developed by the Aberdeen Proving Ground, and our own lysate – using varying ratios of energy mix, lysate, and T7p14 deGFP HP plasmid to evaluate the ideal composition of these components for a cell-free expression kit. We quantify these relationships using fluorescence in order to determine the efficacy of our lysate and the ideal ratio of components for a cell-free, paper-based assay
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    CerviCare: A Point of Care Screening Device for Cervical Precancer
    (iGEM, 2024-04) Bansal, Navya; Firdaus, Sarah; Jocić, Mia; Meyer, Jonathon; Valdés, Trinidad Cubillos; Wu, Jonathan; Jaranson, Renee; Zhang, Kevin; Ferguson, Graham; Adu-Osei, Krista; Namputhiripad, Aditi; Harel, Dana; Lu, Rebecca; Hussain, Haider; Wang, Miranda; Gadigi, Aditri; Senthilkumar, Abhi; Kahn, Jason; Eisenstein, Edward
    Cervical cancer remains a significant health burden, especially in regions with limited access to diagnostic facilities. To combat this, the UMaryland iGEM Team is developing an inexpensive point-of-care cervical precancer screening tool. Utilizing red fluorescent protein (RFP), this tool will provide a reliable color-based output upon detecting specific miRNAs (miR-21, miR-199a, and miR-155-5p) associated with cervical precancer. Our detection approach combines toehold switch and novel synthetic RNA technologies. Toehold switches serve as recognition elements, enabling target miRNA detection with high sensitivity and specificity. Our synthetic RNA ribozyme device will utilize both a novel miRNA sensor and self-cleaving properties to achieve similar sensitivity and specificity. Utilizing two cell-free devices in tandem will allow us to increase the accuracy of our screening device, which will be a paper assay system. Finally, through careful design and optimization, we aim to produce this device at low-cost and simplify it to require minimal training, enabling its use in resource-limited areas.