Smart, biocompatible semi-conductor nanocrystal constructs designed for in-vitro imaging applications
Name
861615617-MIT.pdf
Description
Full printable version
Size
15.16 MB
Format
Adobe PDF
Checksum (MD5)
f906a0aa3faa64e6e3b982871cff9022
Author(s)
Lee, Jungmin, Ph. D. Massachusetts Institute of Technology
Advisor(s)
Moungi G. Bawendi.
Date Issued
2013
Publisher
Massachusetts Institute of Technology
Abstract
Quantum dots (QDs) have unique optical properties that complement fluorescent proteins and organic fluorophores. Despite the widespread use as a fluorescent label in biological imaging studies, the types of biological questions answered by utilizing QDs have been limited due to crucial shortcomings. This thesis focuses on pushing the boundaries of QD applications in vitro, exploring improvements in construct design and methodology to overcome these shortcomings. First, the issues of non-specific binding and reactivity are alleviated by exploring a new method to conjugate molecules onto the QD surface. The improvements that were made enabled a collaborator situated across the country to conjugate biomolecules in a one-step process without performing the usual amine/N-hydroxysuccinimide coupling, thereby diminishing non-specific binding. The utility of QDs in biological applications is further demonstrated by incorporating the nanocrystals into a dynamic sensor construct and taking measurements in a bioenvironment. A dye construct that can act as a Fluorescent Resonant Energy Transfer (FRET) acceptor is conjugated to the FRET donor QD through a molecular linker whose conformation changes depending on the analyte in the microenvironment. As a proof-of-concept, pH is chosen as the environmental factor and the QD-dye FRET sensor is used to track the pH in subcellular compartments along the endocytosis pathway. Lastly, a new microfluidic device is used to deliver QDs into the cell cytosol with high viability and high throughput. QDs delivered this way are shown to be nonaggregated and to interact with the cytosolic environment, opening up the possibility of single molecule tracking of a specific protein of interest inside the cytosol.
Description
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2013.
Cataloged from PDF version of thesis.
Includes bibliographical references.
Subjects
Chemistry.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
M.I.T. theses are protected by
copyright. They may be viewed from this source for any purpose, but
reproduction or distribution in any format is prohibited without written
permission. See provided URL for inquiries about permission.
copyright. They may be viewed from this source for any purpose, but
reproduction or distribution in any format is prohibited without written
permission. See provided URL for inquiries about permission.
Persistent DSpace Link
