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Construction and Characterization of a Single-Chain Variable Fragment Antibody Library against Fusobacterium nucleatum

dc.contributor.copyright-releaseNot Applicableen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.departmentDepartment of Microbiology & Immunologyen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.external-examinerDr. Nikhil Thomasen_US
dc.contributor.graduate-coordinatorDr. Brent Johnstonen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.thesis-readerDr. Stephen Bearneen_US
dc.contributor.thesis-readerDr. Yung- Hua Lien_US
dc.contributor.thesis-supervisorDr. Song Lee and Dr. Scott Halperinen_US
dc.date.accessioned2012-08-09T16:55:53Z
dc.date.available2012-08-09T16:55:53Z
dc.date.defence2012-07-26
dc.date.issued2012-08-09
dc.descriptionFarhan Khan placed second in the International Association for Dental Research/Unilever Hatton Competition in the Senior Basic Science Research Category representing Canada, while presenting the research contained in this dissertation. This international competition took place during the 90th General Session & Exhibition of the International Association for Dental Research in Iguaçu Falls, Brazil in June 2012.en_US
dc.description.abstractDental plaque forms sequentially, with Fusobacterium nucleatum facilitating the adhesion of pathogenic late colonizers. We hypothesize that a single-chain variable fragment (scFv) antibody library will enable the identification of F. nucleatum adhesins and help elucidate the molecular mechanisms of coaggregation between F. nucleatum and other bacteria. A 4X10^8 clones scFv phage display library was created using spleen RNA from a mouse immunized with F. nucleatum. The library was enriched by biopanning against F. nucleatum 6 times and 292 individual clones tested by ELISA reacted strongly to F. nucleatum. Sixty-two of those clones inhibited F. nucleatum coaggregation with Streptococcus sanguinus. Analysis of select clones revealed differences in coaggregation inhibition, recognition of outer membrane proteins, and BstOI restriction pattern. DNA sequencing showed 6 unique scFvs and of them 3 strongly inhibited interaction with 5 Streptococcus species. These scFvs recognize the outer membrane autotransporter protein RadD (Fn1526), as determined by mass spectrometry.en_US
dc.identifier.urihttp://hdl.handle.net/10222/15184
dc.language.isoenen_US
dc.subjectFusobacterium nucleatumen_US
dc.subjectCoaggregationen_US
dc.subjectBiofilmen_US
dc.subjectAntibody Libraryen_US
dc.subjectPeriodontal diseaseen_US
dc.subjectDental cariesen_US
dc.subjectSingle-Chain Variable Fragmenten_US
dc.subjectAdhesinen_US
dc.subjectRadDen_US
dc.subjectFn1526en_US
dc.titleConstruction and Characterization of a Single-Chain Variable Fragment Antibody Library against Fusobacterium nucleatumen_US

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