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Massachusetts Institute of Technology

Microsystems platforms for array-based single-cell biological assays

Abstract

dc:description.abstract

For much of the past century, plated cell cultures have served investigations regarding a variety of fundamental biological processes. Though this in vitro approach has been fruitful, for surveying topics including cell cycle effects3' 8, pro-survival4, 7, 9, 10 and apoptotic2' 11 signaling networks, gene regulationl2' 13, and stress dynamicsl4' 15 (among others), it caters best to harvesting the averaged responses from binned populations of cells and offers only limited avenues for tracking individual cell behaviors. Microsystems-based initiatives16-28 are beginning to aid this investigative shortcoming by offering a variety of strategies for handling individual cells. Such efforts, may ultimately serve studies of cross-population heterogeneity29-33, an effect often masked when tracking responses via averaged population-based means. As it is believed that small subpopulations of cells may be responsible or determining the fate of various diseases and developmental processes34-36, this new paradigm for probing cell function will likely offer key insights.In my dissertation, I offer a unique suite of microsystems-based tools37-42 for servicing novel biological assays centered on cross-population dynamics. This work leverages the investigative potential enabled by arrayed groupings of precisely-spaced single cells and presents innovations in active and passive cell trapping architectures, packaging design, and the use of novel materials for microfabrication41' 43. From proof-of-concept forays, where I discuss the first reported row/column-based electrically-addressable platform40 for trapping, imaging, and releasing collections of individual cells, to scaled implementations that employ frequency modulation to assign unique forcing effects to in-system constructs, I outlay fundamentals for designing, building, and evaluating dielectrophoresis-reliant (DEP) microsystems architectures.

Degree

thesis:*
Department dc:contributor.department
Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2008

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Taff, Brian M., 1978-
Advisor dc:contributor.advisor
  • Joel Voldman.

Subjects

dc:subject × 1

Rights

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.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/45879
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/45879

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Taff, Brian M., 1978-. Microsystems platforms for array-based single-cell biological assays. Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/45879