Cell-free synthetic biology for affordable, on-demand diagnostics
Name
1144858739-MIT.pdf
Size
15.64 MB
Format
Adobe PDF
Checksum (MD5)
c178b1299b195e59987ceaabe980821c
Author(s)
Dy, Aaron J.(Aaron James)
Advisor(s)
James J. Collins and Domitilla Del Vecchio.
Date Issued
2019
Publisher
Massachusetts Institute of Technology
Abstract
Detection of biomarkers, such as nucleic acids, performs critical roles in managing infectious disease outbreaks, point-of-care testing, and public health monitoring. However, many diseases and public health problems suffer from a lack of affordable, portable tests that can be used to sensitively detect nucleic acids and respond in a rapid manner. Current methods to nucleic acid testing are too expensive, slow, and complex to be routinely used outside of specialized lab settings. New diagnostic tools are needed that can work in resource-limited settings to help guide prompt treatment decisions, prevent spread of infectious diseases, and inform public health decisions. Cell-free synthetic biology has shown promise as a portable, affordable technology to detect biomolecules like nucleic acids. In this thesis, I present several advancements to cell-free synthetic biology diagnostics that enable new application areas. First, I present a paper-based cell-free synthetic biology platform using RNA toehold switch sensors to detect RNAs from human gut microbiome. We showed that this method could quantify bacterial and human RNA transcripts comparably to gold standard methods while reducing time and cost. Next, I used similar cell-free detection technology to create a set of fruit DNA-sensing demonstrations that can be used in high school biology classrooms. I then sought to engineer biomolecular circuits that can process multiple sensor inputs to reduce cost, improve specificity, and build classifier circuits. Finally, I present work to develop and use clustered regularly interspaced short palindromic repeats (CRISPR) enzyme-based diagnostics to achieve attomolar sensitivity and single-nucleotide mismatch specificity. Together, these projects demonstrate a set of advancements in cell-free synthetic biology diagnostics toward filling the gap of nucleic acid detection technologies that are low-cost, portable, sensitive, and easy to use.
Description
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biological Engineering, 2019
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 104-116).
Subjects
Biological Engineering.
MIT Department
Massachusetts Institute of Technology. Department of Biological Engineering
Terms of Use
MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.
Persistent DSpace Link
