Abstract
dc:description.abstractThis thesis presents a novel microfluidic platform for investigating cellular signaling networks, combining a programmable system for generating arbitrarily complex temporal input stimulant concentration profiles with real-time fluorogenic monitoring of cell physiological response. While cellular assay automation has been demonstrated in microfluidic devices, applying microfluidics to more difficult, multi-parametric systems biology problems, like the analysis of signal transduction pathways, requires a higher level of automation to rigorously control environmental parameters and detect output signals. Addressing this challenge, I developed a JAVA-based programmable microvalve system for automated control of reagent delivery enabling the end user to generate complex chemical waveforms and perform multiple assays on individually addressable cell chambers on chip. Typically, signaling behavior has been inferred from cellular responses to step inputs or slow square waves [1-3]. Generation of arbitrary waveforms in these experiments involved either complex programmable syringe pump systems or physically moving a sample through a spatial gradient to create temporal changes [4, 5]. My device used computer-controlled elastomer valves to dynamically generate arbitrary concentration profiles with waveform periodicities as short as 10 seconds. This kind of complex signal input to cellular networks has not previously been reported. To demonstrate this platform, experiments were performed monitoring the change of intracellular free calcium in response to the application of histamine. Cells were treated with a dye that fluoresces only when bound to calcium within the cytosolic compartment.
Degree
thesis:*- Department dc:contributor.department
- Massachusetts Institute of Technology. Dept. of Mechanical Engineering.
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2008
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Craig, David, S.M. Massachusetts Institute of Technology
- Advisor dc:contributor.advisor
-
- Todd Thorsen.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- 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.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/1721.1/44871
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/44871