C60 Amino Acids and Peptides

dc.contributor.advisorBarron, Andrew R.en_US
dc.creatorStrom, T. Amandaen_US
dc.date.accessioned2013-03-08T00:39:16Zen_US
dc.date.available2013-03-08T00:39:16Zen_US
dc.date.issued2011en_US
dc.description.abstractSince the discovery of the buckyball in 1985, researchers have imagined its potential in fields ranging from materials science to medicinal chemistry. The unique size, shape and hydrophobicity of C 60 fullerene endow it with the ability to interact with biological superstructures such as enzymes and membranes making it attractive as a potential pharmacophore. In this regard, we have developed a new, simple route to water soluble fullerene amino acids, both alkyl and aryl, through the dipolar addition of azido starting materials. The synthesis of our phenylalanine derivative, including the chromatographic purification, requires only one day for its completion. We have subsequently used our C 60 phenylalanine derivative in the synthesis of a series of C 60 peptides for the purposes of enzyme inhibition, specifically human immunodeficiency virus Type 1 protease, a critical viral enzyme responsible for the maturation of the virus and a popular target of medicinal chemists. We have demonstrated the ability of our C 60 amino acids and peptides to inhibit HIV-1 PR in a cell-free fluorescence based assay at low nanomolar concentrations. Graphite, or specifically graphene, has recently come to the forefront of nanomaterials research due to it similar scale, properties, and reaction pathways as other more costly carbon nanostructures such as carbon nanotubes. We have demonstrated the high yield functionalization of graphitic starting materials through the thermal decomposition of azido amino acids to their corresponding nitrene. The result is an inexpensive, highly functionalized, carbon based scaffold.en_US
dc.format.extent126 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.callnoTHESIS CHEM. 2011 STROMen_US
dc.identifier.citationStrom, T. Amanda. "C60 Amino Acids and Peptides." (2011) Diss., Rice University. <a href="https://hdl.handle.net/1911/70455">https://hdl.handle.net/1911/70455</a>.en_US
dc.identifier.digitalStromTen_US
dc.identifier.urihttps://hdl.handle.net/1911/70455en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectPure sciencesen_US
dc.subjectFullerenesen_US
dc.subjectAmino acidsen_US
dc.subjectProtease inhibitorsen_US
dc.subjectGrapheneen_US
dc.subjectOrganic chemistryen_US
dc.titleC60 Amino Acids and Peptidesen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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