Files in this item



application/pdf3362774.pdf (4MB)Restricted to U of Illinois
(no description provided)PDF


Title:Biochemical Investigation of the Intracellular Trafficking of Non-Viral and Hybrid Gene Therapy Vectors
Author(s):Drake, David Michael
Doctoral Committee Chair(s):Daniel Wayne Pack
Department / Program:Chemical Engineering
Discipline:Chemical Engineering
Degree Granting Institution:University of Illinois at Urbana-Champaign
Subject(s):Biology, Cell
Abstract:We also used reverse transcriptase inhibitor 3'-azido-3'-deoxythymidine (AZT) applied of post-transfection time increments to determine the timeframe of reverse transcription, thereby estimating endosomal escape of VLP. MLV were observed to achieve reverse transcription rapidly, with more than half of infecting viruses being reverse transcribed within 8 hours. PEI:VLP were delayed approximately 4 hours (relative to viruses) in having their RNA reverse transcribed. This suggests VLP experience delayed endosomal escape, unpackaging, or release of the capsid/reverse transcription complex from the lipid bilayer. This delay likely accounts for much of the inefficiency observed in PEI:VLP relative to MLV. (Similar experiments attempted with integrase inhibitors did not yield useful results.) Improvement of hybrid vectors probably depends on expediting the escape of VLP from the endolysosomal network and the VLP lipid bilayer. This might be accomplished by developing polymers with stronger endosomolytic properties and/or by the incorporation of fusogenic peptides to assist in endosome and bilayer escape.
Issue Date:2009
Description:188 p.
Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2009.
Other Identifier(s):(MiAaPQ)AAI3362774
Date Available in IDEALS:2015-09-25
Date Deposited:2009

This item appears in the following Collection(s)

Item Statistics