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dc.contributor.advisorAngela M. Belcher.en_US
dc.contributor.authorLee, Soo-Kwanen_US
dc.contributor.otherMassachusetts Institute of Technology. Biological Engineering Division.en_US
dc.date.accessioned2007-08-03T18:18:20Z
dc.date.available2007-08-03T18:18:20Z
dc.date.copyright2006en_US
dc.date.issued2006en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/38241
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.en_US
dc.descriptionIncludes bibliographical references (leaves 86-96).en_US
dc.description.abstractFilamentous bacteriophage (M13) are excellent biological build block due to their multiple peptide display system including type 8 (complete peptide display at pVIII) and type 83 (complete peptide display at both pVIII and pIII) display systems. Unlike the phagemid systems, the advantage of these systems is that we can get homogenous peptide display on pVIII resulting in uniform placement of selected molecules as well as defined length and width. In this thesis, type 8 and type 83 phage were constructed and used as biological scaffolds to meet the following four specific aims. First, the self-assembly of engineered M13 bacteriophage as a template for Co-Pt crystals was demonstrated. An phage library with an octapeptide library on the major coat protein (pVIII) was used for selection of binders to cobalt ions. Fibrous structures with directionally ordered phage were obtained by interaction with cobalt ions. Co-Pt alloys were synthesized on the fibrous scaffold, and their magnetic properties were characterized. The mineralization showed organized nanoparticles on fibrous bundles with superparamagnetic properties. Second, an in vitro molecular selection method in non-biological conditions for inorganic synthesis was introduced.en_US
dc.description.abstract(cont.) A phage display peptide library which is resistant to ethanol was constructed and used for selection against titania in 90% ethanol. The selected peptide, with a conserved basic amino acid sequence, promotes nanoparticle formation (- 60 nm) during titania synthesis by the traditional sol-gel method. Third, storage of proteins in smectically aligned phage film was demonstrated. [Beta]-galactosidase and a green fluorescent protein variant were stored in the phage film with increased stability. In addition, streptavidin conjugated phycoerythrin were aligned in a SI phage film, in which streptavidin binding peptides are displayed at the end of the phage particles. The alignment showed increased fluorescent intensity of phycoerythrin molecules. Finally, the potential of type 8 and type 83 phage as a nano-structural scaffold were studied 'or device application. An Au binding peptide was selected using type 8 phage library. Self-assembly of gold particles on phage was observed. In addition, type 83 phage which display both streptavidin binding peptide at pIII and Au binding peptide at pVIII were constructed for complex assembly of both Au nanoparticles and streptavidin conjugated nanoparticles. Genetically engineered bacteriophage show promise for application including biologically compatible materials and functional bio-inorganic hybrid materials.en_US
dc.description.statementofresponsibilityby Soo-Kwan Lee.en_US
dc.format.extent96 leavesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectBiological Engineering Division.en_US
dc.titleGenetic engineering of bacteriophage and its applications for biomimetic materialsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.identifier.oclc146310843en_US


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