Expanding the capabilities of biosensors with novel molecular switches

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Abstract/Contents

Abstract
Biosensors capable of tracking the body's molecular state have tremendous potential to improve lives by making healthcare more accessible, personalized, and preventative. At the same time, developing biosensors that are both compatible with point-of-care or continuous monitoring and can accurately track a wide range of clinically important biomarkers poses a tremendous technical challenge. These sensors must operate without the sample processing employed by conventional laboratory diagnostic assays and must measure targets rapidly with molecular sensitivity and specificity within complex biofluid samples. These demands may be met by biosensors based on "molecular switches" -- engineered receptors that bind molecular targets with high specificity and undergo a binding-induced conformational change that produces measurable optical or electronic signals. However, to date these molecular switch biosensors have remained limited to sensing only a handful of molecules. It remains an outstanding challenge to develop generalizable strategies to methods for engineering molecular switches to sense the complete range of health biomarkers. In this dissertation, I begin by considering how we can develop sensors that are compatible with real world, day-to-day use. I analyze the diagnostic value of biosensing in dermal interstitial fluid, a biofluid with emerging interest for use with minimally invasive and continuous wearable sensors. The remainder of the dissertation focuses on three projects where I expand the generalizability molecular switches, enabling more rapid development of biosensors for new biomarker targets. In the first project, I introduce an approach for engineering off-the-shelf antibodies into antibody-based molecular switches that achieve continuous optical biosensing by augmenting them with a rationally designed DNA-linked competitor molecule. In the second project, I develop a universal protein-based competitor molecule that provides an even more universal method for our antibody-based molecular switch design to be applied to sensing new targets. In the third project, I develop a rational design approach for engineering DNA-based molecular switches that have pH-dependent properties which can be tailored to improve biosensor performance, and for potential drug delivery applications. Taken together, these advances in molecular switch design offer a toolkit of generalizable strategies that can be used to develop next-generation biosensors which sense a wide range of biomarkers for addressing a wide range of clinical needs.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2023; ©2023
Publication date 2023; 2023
Issuance monographic
Language English

Creators/Contributors

Author Thompson, Ian Andrew Paul
Degree supervisor Soh, H. Tom
Thesis advisor Soh, H. Tom
Thesis advisor Huang, Possu
Thesis advisor Wang, Shan X
Degree committee member Huang, Possu
Degree committee member Wang, Shan X
Associated with Stanford University, School of Engineering
Associated with Stanford University, Department of Electrical Engineering

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Ian Thompson.
Note Submitted to the Department of Electrical Engineering.
Thesis Thesis Ph.D. Stanford University 2023.
Location https://purl.stanford.edu/kp819qg9366

Access conditions

Copyright
© 2023 by Ian Andrew Paul Thompson
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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