Show simple item record

dc.contributor.authorAbdul Rehman, Sohaib
dc.date.accessioned2019-09-05T13:59:12Z
dc.date.available2019-09-05T13:59:12Z
dc.date.issued2019-10-26
dc.date.submitted2019-03-13
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/296453
dc.description.abstractThis thesis describes the design, development and optimisation of a multifunctional localisation based super-resolution microscope at Cambridge Advanced Imaging Centre. The microscope is optimised to perform single and dual-colour imaging with high localisation precision and accuracy. Moreover, three-dimensional imaging capability is included in the microscope using the double-helix point spread function and the light field imaging modality. The thesis also describes the application of the microscope to image challenging biological samples, in collaboration with the research groups at the Department of Physiology, Development and Neuroscience. This includes, studying dynamics of a DNA-binding transcription factor for the Notch signalling pathway, deep within the whole salivary glands of Drosophila. Characterisation and optimisation of the microscope and the subsequent image analysis pipeline, to extract dynamics of single molecules at such depths is also discussed. Another application of the microscope, discussed in the thesis, is the study of chromatin architecture in primary spermatocytes of Drosophila. This includes optimisation of imaging conditions and data analysis software to reconstruct features with different densities of labelling dye in the imaged nuclei. Calibration and application of dual-colour localisation microscopy, to visualise the arrangement of active transcription sites in chromatin fibres is also discussed. Finally, the thesis also presents the application of light field imaging technique to extend the depth of field of localisation microscopy to over 20 μm. Modification of the microscope for light field imaging and a method to localise point emitters with high precision in all three spatial dimensions is discussed. The effectiveness of the technique for single molecule imaging is shown by detecting emissions from single fluorophores in labelled cells.
dc.language.isoen
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectFluorescence Microscopy
dc.subjectSuper-resolution Microscopy
dc.subjectLocalisation Microscopy
dc.subjectThree-dimensional Microscopy
dc.subjectLightfield Microscopy
dc.subjectSingle Molecule Tracking
dc.subjectClustering
dc.subjectNotch Pathway
dc.subjectChromatin Architecture
dc.subjectOptics
dc.titleSuper-resolution Microscopy: Novel Developments and Optimisations
dc.typeThesis
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (PhD)
dc.publisher.institutionUniversity of Cambridge
dc.publisher.departmentPhysiology, Development and Neuroscience
dc.date.updated2019-09-05T10:22:55Z
dc.identifier.doi10.17863/CAM.43503
dc.contributor.orcidAbdul Rehman, Sohaib [0000-0002-1170-6610]
dc.publisher.collegeJesus College
dc.type.qualificationtitlePhD in Super-resolution Microscopy
cam.supervisorO'Holleran, Kevin
cam.supervisorLee, Steven F.
cam.supervisor.orcidO'Holleran, Kevin [0000-0003-1039-2127]
cam.supervisor.orcidLee, Steven F. [0000-0003-4492-5139]
cam.thesis.fundingfalse


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
Except where otherwise noted, this item's licence is described as Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)