Title:
DNA Nanotechnology to Map and Manipulate Adhesion Forces at Fluid Interfaces

dc.contributor.advisor Salaita, Khalid
dc.contributor.author Glazier, Roxanne
dc.contributor.committeeMember Curtis, Jennifer
dc.contributor.committeeMember García,, Andrés
dc.contributor.committeeMember Marcus, Adam
dc.contributor.committeeMember Santangelo, Philip
dc.contributor.department Biomedical Engineering (Joint GT/Emory Department)
dc.date.accessioned 2021-06-10T13:53:10Z
dc.date.available 2021-06-10T13:53:10Z
dc.date.created 2020-05
dc.date.issued 2020-03-27
dc.date.submitted May 2020
dc.date.updated 2021-06-10T13:53:11Z
dc.description.abstract Cells transmit piconewton (pN) receptor forces to ligands in the extracellular matrix (ECM) and on the surface of adjacent cells. These forces regulate functions ranging from adhesion to clotting and the immune response. Whereas adhesion mechanics on rigid substrates are well characterized, understanding mechanotransduction at cell-cell junctions remains challenging due to a lack of tools. We develop and apply new classes of DNA-based force probes to map and manipulate receptor forces on supported lipid bilayers (SLBs), planar membranes that mimic an adjacent cell. We use these probes to elucidate force balance in podosomes, which are multipurpose protrusive structures that form at cell-cell and cell-ECM interfaces. Podosomes have a core-ring architecture, and previous works demonstrated that the podosome’s actin core generates nanonewton protrusive forces. However, the podosome’s contractile landscape remained poorly understood. In Aim 1 (Chapter 3), we develop and apply Molecular Tension- Fluorescence Lifetime Imaging Microscopy to map integrin receptor forces and clustering on SLBs. We demonstrate that integrin receptors apply pN tension in podosome rings. We then introduce photocleavable probes to site-specifically perturb adhesion forces and apply rupturable DNA-based force probes to test the role of receptor tension in podosome formation and maintenance. These studies confirm a local mechanical feedback between podosome core protrusion and integrin receptor tension. In Aim 2 (Chapter 4), we evaluate structure and energy transfer across a library of DNA-based tension probes using spectroscopy and microscopy. We then demonstrate the functional implications of probe design on cellular imaging. This work expands our understanding of receptor forces in podosome mechanobiology and contributes new insight and tools for studying juxtacrine receptor interactions.
dc.description.degree Ph.D.
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/64589
dc.language.iso en_US
dc.publisher Georgia Institute of Technology
dc.subject Mechanotransduction
dc.subject Integrins
dc.subject Biomembranes
dc.subject Podosomes
dc.subject Adhesion
dc.subject Mechanobiology
dc.subject Molecular probes
dc.title DNA Nanotechnology to Map and Manipulate Adhesion Forces at Fluid Interfaces
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Salaita, Khalid
local.contributor.corporatename Wallace H. Coulter Department of Biomedical Engineering
local.contributor.corporatename College of Engineering
relation.isAdvisorOfPublication 473078da-e893-44af-8f0f-7a8cda93d9f5
relation.isOrgUnitOfPublication da59be3c-3d0a-41da-91b9-ebe2ecc83b66
relation.isOrgUnitOfPublication 7c022d60-21d5-497c-b552-95e489a06569
thesis.degree.level Doctoral
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