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dc.contributor.advisorDholakia, Kishan
dc.contributor.authorMitchell, Claire A.
dc.coverage.spatial248en_US
dc.date.accessioned2015-03-25T16:05:33Z
dc.date.available2015-03-25T16:05:33Z
dc.date.issued2015-06-24
dc.identifier.urihttp://hdl.handle.net/10023/6328
dc.description.abstractOptical cell manipulation allows precise and non-invasive exploration of mammalian cell function and physiology for medical applications. Plants, however, represent a vital component of the Earth’s ecosystem and the knowledge gained from using optical tools to study plant cells can help to understand and manipulate useful agricultural and ecological traits. This thesis explores the potential of several biophotonic techniques in plant cells and tissue. Laser-mediated introduction of nucleic acids and other membrane impermeable molecules into mammalian cells is an important biophotonic technique. Optical injection presents a tool to deliver dyes and drugs for diagnostics and therapy of single cells in a sterile and interactive manner. Using femtosecond laser pulses increases the tunability of multiphoton effects and confines the damage volume, providing sub-cellular precision and high viability. Extending current femtosecond photoporation knowledge to plant cells could have sociological and environmental benefits, but presents different challenges to mammalian cells. The effects of varying optical and biological parameters on optical injection of a model plant cell line were investigated. A reconfigurable optical system was designed to allow easy switching between different spatial modes and pulse durations. Varying the medium osmolarity and optoinjectant size and type affected optoinjection efficacy, allowing optimisation of optical delivery of relevant biomolecules into plant cells. Advanced optical microscopy techniques that allow imaging beyond the diffraction limit have transformed biological studies. An ultimate goal is to merge several biophotonic techniques, creating a plant cell workstation. A step towards this was demonstrated by incorporating a fibre-based optical trap into a commercial super-resolution microscope for manipulation of cells and organelles under super-resolution. As proof-of-concept, the system was used to optically induce and quantify an immunosynapse. The capacity of the super-resolution microscope to resolve structure in plant organelles in aberrating plant tissue was critically evaluated.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectBiophotonicsen_US
dc.subjectPlant cellsen_US
dc.subjectPhotoporationen_US
dc.subjectUltrafast lasersen_US
dc.subjectSuper-resolution microscopyen_US
dc.subjectOptical trappingen_US
dc.subject.lccTK8360.O69M5
dc.subject.lcshOptical tweezersen_US
dc.subject.lcshTransfectionen_US
dc.subject.lcshPlant cells and tissuesen_US
dc.subject.lcshFemtosecond lasersen_US
dc.titlePhotoporation and optical manipulation of plant and mammalian cellsen_US
dc.typeThesisen_US
dc.contributor.sponsorEngineering and Physical Sciences Research Council (EPSRC)en_US
dc.contributor.sponsorJames Hutton Instituteen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.publisher.departmentJames Hutton Instituteen_US


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