Title page for ETD etd-02092007-153948


Type of Document Dissertation
Author Reidy, Michael James
URN etd-02092007-153948
Title Engineering of the RTB Lectin as a Carrier Platform for Proteins and Antigens
Degree PhD
Department Plant Pathology, Physiology, and Weed Science
Advisory Committee
Advisor Name Title
Cramer, Carole L. Committee Co-Chair
Nessler, Craig L. Committee Co-Chair
Bevan, David R. Committee Member
Gillaspy, Glenda E. Committee Member
Medina-Bolivar, Fabricio Committee Member
Keywords
  • adjuvant
  • lectin-mediated uptake
  • Immunoglobulin scaffolding
  • Type II RIP processing
  • lectin
  • drug carrier
  • N. benthamiana
  • ricin B-chain
  • capture/carry platform
  • Ricin
  • retrograde trafficking
  • RTB
  • plant-based bioproduction
  • Agrobacterium-mediated transient expression
  • antigen carrier
Date of Defense 2007-01-26
Availability unrestricted
Abstract
The major obstacle many promising drugs struggle to overcome is the barrier imposed by the outer cell membrane. In addition to technologies such as liposomes and cell-penetrating peptides, more attention is being given to the class of proteins known as lectins to deliver therapeutic and antigenic proteins to the interiors of cells. Lectins bind to but do not modify sugars, and provide an efficient route to endocytosis. The galactose/N-acetyl-galactosamine specific lectin ricin B-chain (RTB) is especially attractive in possibly fulfilling a carrier role due to its well-characterized endocytotic trafficking and its efficacy over a wide range of cell types. By producing RTB recombinantly in plants it is possible to create a fully active, non-toxic carrier that does not rely on the processing of large amounts of toxic material (e.g. castor bean). Payload molecules such as small molecules and proteins can be attached to RTB via chemical conjugation at primary amine groups, without the loss of lectin or uptake activities. The biotin/streptavidin interaction and direct genetic fusion of polypeptides also provide efficient mechanisms for the attachment of payload proteins to RTB. An immunoglobulin domain-based scaffolding mechanism bridges modified RTB and payload proteins when co-expressed in Agrobacterium-infiltrated plant leaves. Carrier and payload proteins expressed in plants and E. coli, respectively, and purified independently are not able to assemble into an efficient carrier/payload arrangement. These findings show that plant cells are able to correctly produce the two components of the carrier/payload system and assemble them into an efficient and flexible capture and carry technology.
Files
  Filename       Size       Approximate Download Time (Hours:Minutes:Seconds) 
 
 28.8 Modem   56K Modem   ISDN (64 Kb)   ISDN (128 Kb)   Higher-speed Access 
  Michael_Reidy_Dissertation_4.pdf 10.17 Mb 00:47:05 00:24:12 00:21:11 00:10:35 00:00:54

Browse All Available ETDs by ( Author | Department )

dla home
etds imagebase journals news ereserve special collections
virgnia tech home contact dla university libraries

If you have questions or technical problems, please Contact DLA.