Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2007. === Includes bibliographical references. === The study of proteins in biological systems requires a comprehensive approach: investigating dynamics, interaction and identification. This...

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Main Author: Anwar, Moshiur Mekhail
Other Authors: Paul Matsudaira.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2008
Subjects:
Online Access:http://hdl.handle.net/1721.1/42229
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-422292019-05-02T16:02:48Z Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction Technologies for the study of protein dynamics, detection and interaction Anwar, Moshiur Mekhail Paul Matsudaira. Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science. Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science. Electrical Engineering and Computer Science. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2007. Includes bibliographical references. The study of proteins in biological systems requires a comprehensive approach: investigating dynamics, interaction and identification. This thesis will examine several technological approaches we have developed to address these needs. To enable the study of the dynamics of biological systems, we have developed a method for using atomic force microscopy (AFM) to image motion on an angstrom scale with microsecond time resolution. As proteins move, diffuse, or are actively trafficked within the cellular environment, they interact with other biological molecules. Protein microarrays offer a high-throughput method of investigating these protein interactions, but their use has largely been hindered by the need to clone and purify thousands of proteins. We have developed a novel technique to pattern proteome-scale microarrays using a cellular lysate, whereby all relevant proteins are synthesized with the correct post-translational modifications. Additionally, we have integrated the identification of proteins with quantitative mass spectrometry (SILAC). Using these arrays we have probed changes in the phosphorylation state of cells in response to activation of the Erb1 and Erb2 receptors. Using our microarray platform we were able to further probe the phosphoproteome for proteins that have multiple post-translational modifications. The widespread use of protein, DNA and small molecule microarrays has been limited in clinical and diagnostic settings due to the cost of microarray readers. Therefore, we have developed an optics-free integrated circuit-based microarray imaging chip that is compatible with existing (optics-based) microarray protocols. By eliminating optics, and developing the reader using integrated circuit technology, the cost can be significantly reduced. The reader is powered by a single sine wave, enabling a wireless interface. We use this reader to detect a biotin-streptavidin interaction using standard microarray procedures. by Moshiur Mekhail Anwar. Ph.D. 2008-09-03T15:00:38Z 2008-09-03T15:00:38Z 2007 2007 Thesis http://hdl.handle.net/1721.1/42229 231358030 eng 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. http://dspace.mit.edu/handle/1721.1/7582 2 v. (207 leaves) application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Electrical Engineering and Computer Science.
spellingShingle Electrical Engineering and Computer Science.
Anwar, Moshiur Mekhail
Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2007. === Includes bibliographical references. === The study of proteins in biological systems requires a comprehensive approach: investigating dynamics, interaction and identification. This thesis will examine several technological approaches we have developed to address these needs. To enable the study of the dynamics of biological systems, we have developed a method for using atomic force microscopy (AFM) to image motion on an angstrom scale with microsecond time resolution. As proteins move, diffuse, or are actively trafficked within the cellular environment, they interact with other biological molecules. Protein microarrays offer a high-throughput method of investigating these protein interactions, but their use has largely been hindered by the need to clone and purify thousands of proteins. We have developed a novel technique to pattern proteome-scale microarrays using a cellular lysate, whereby all relevant proteins are synthesized with the correct post-translational modifications. Additionally, we have integrated the identification of proteins with quantitative mass spectrometry (SILAC). Using these arrays we have probed changes in the phosphorylation state of cells in response to activation of the Erb1 and Erb2 receptors. Using our microarray platform we were able to further probe the phosphoproteome for proteins that have multiple post-translational modifications. The widespread use of protein, DNA and small molecule microarrays has been limited in clinical and diagnostic settings due to the cost of microarray readers. Therefore, we have developed an optics-free integrated circuit-based microarray imaging chip that is compatible with existing (optics-based) microarray protocols. By eliminating optics, and developing the reader using integrated circuit technology, the cost can be significantly reduced. The reader is powered by a single sine wave, enabling a wireless interface. We use this reader to detect a biotin-streptavidin interaction using standard microarray procedures. === by Moshiur Mekhail Anwar. === Ph.D.
author2 Paul Matsudaira.
author_facet Paul Matsudaira.
Anwar, Moshiur Mekhail
author Anwar, Moshiur Mekhail
author_sort Anwar, Moshiur Mekhail
title Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
title_short Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
title_full Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
title_fullStr Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
title_full_unstemmed Enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
title_sort enabling tools for biological analysis : technologies for the study of protein dynamics, detection and interaction
publisher Massachusetts Institute of Technology
publishDate 2008
url http://hdl.handle.net/1721.1/42229
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