Extended transient transfection by repeated delivery of in vitro-transcribed RNA

Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2008.

Bibliographic Details
Main Author: Angel, Matthew
Other Authors: Mehmet F. Yanik.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2009
Subjects:
Online Access:http://hdl.handle.net/1721.1/47895
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author Angel, Matthew
author2 Mehmet F. Yanik.
author_facet Mehmet F. Yanik.
Angel, Matthew
author_sort Angel, Matthew
collection MIT
description Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2008.
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spelling mit-1721.1/478952019-04-10T14:26:26Z Extended transient transfection by repeated delivery of in vitro-transcribed RNA Angel, Matthew Mehmet F. Yanik. 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 (S.M.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2008. Includes bibliographical references (p. 53-56). An experimental study was performed to evaluate a novel method of controlling protein expression by repeatedly transfecting cells with in vitro-transcribed RNA. Transcripts encoding six factors, each known to play an important role in cell-type specification and maintenance, were designed and synthesized. Aspects of the design were optimized, and the intracellular stability and translation efficiency of the ivT RNA were quantified. Transcripts were delivered to cells by electroporation, and a method of increasing the rate at which cells recover from ivT-RNA transfection by combined knockdown of innate-immune-related genes was developed. Using this technique a high, approximately steady-state level of protein expression was transduced in MRC-5 human fetal-lung fibroblasts by repeated transfection with capped, poly(A)+ ivT RNA encoding a protein with an intracellular half-life of approximately three days. Transfection at 24-hour intervals with ivT RNA encoding a less stable protein resulted in protein expression that peaked twelve hours after each transfection, and diminished before the next transfection. In both cases, cells sustained a high rate of proliferation. In this study, extended transient transfection by repeated delivery of ivT RNA was shown to transduce expression of defined factors in cultured cells without genetic modification or the extensive screening required in small-molecule approaches and with significant control over the level of transduced protein. This technique may become a powerful tool in the development of new directed-differentiation and cell-type-conversion protocols. by Matthew Angel. S.M. 2009-10-01T16:00:02Z 2009-10-01T16:00:02Z 2008 2008 Thesis http://hdl.handle.net/1721.1/47895 435528760 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 56 p. application/pdf Massachusetts Institute of Technology
spellingShingle Electrical Engineering and Computer Science.
Angel, Matthew
Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title_full Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title_fullStr Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title_full_unstemmed Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title_short Extended transient transfection by repeated delivery of in vitro-transcribed RNA
title_sort extended transient transfection by repeated delivery of in vitro transcribed rna
topic Electrical Engineering and Computer Science.
url http://hdl.handle.net/1721.1/47895
work_keys_str_mv AT angelmatthew extendedtransienttransfectionbyrepeateddeliveryofinvitrotranscribedrna