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Interrogations of protein and RNA: localisation, interactions and dynamics 10.17863/CAM.66425 Elzek, Mohamed Lilley, Kathryn 0000000305946543 Willis, Anne Eukaryotic cells are characterised by a high degree of structural partitioning into distinct microenvironments dedicated to diverse and specific roles. To maintain these microenvironments, the functions of endogenous RNAs and proteins are fine-tuned by a set of. post-transcriptional and post-translational regulation mechanisms fundamental to complex cellular processes, throughout the stages of development or in response to acute stimuli. Whereas microscopy- or affinity-based methods are routinely employed to determine the location or the interactions of a limited number of proteins or RNAs, a system-wide analysis enables a thorough understanding of the functional and spatial dynamics of the proteome and transcriptome. In this Thesis, two biochemical fractionation-based techniques were developed in the quest for subcellular exploration of the proteome and transcriptome. In addition, two biological questions were investigated with regard to the post-transcriptional control of the ultraviolet irradiation induced stress response and stem cell pluripotency phase transition. In Chapter 3, a one-step subcellular fractionation procedure using multiple iodixanol containing gradients, termed “MultiLOPIT”, is presented, which provides high-resolution organelle resolution for comparative applications in different cell states or conditions. In Chapter 4, characterisation of the dynamics of protein and RNA-binding proteins, post-translational modification, and spatiotemporal localisation are investigated in response to UV-induced cellular stress. This multi-omics approach highlights selective cytosolic translation programmes and chaperone machinery upon UV irradiation. Chapter 5 describes an efficient, high-throughput and scalable method for simultaneous mapping of the subcellular transcriptome, proteome and RBPome. Finally, chapter 6 delineates the dynamics of the post-transcriptional regulatory programmes mediated with RBPs, highlighting ribosome biogenesis and splicing mechanism involvement through the exit of naïve pluripotency. The results of the research in this Thesis offer a strong basis for the application of localisation, interactions and dynamics studies of RNA and proteins, which enable multi-layered system-level interrogations of cell biology. University of Cambridge 2020-09-30 Thesis Doctoral Doctor of Philosophy (PhD) eng MRC medical research foundation BP Egypt https://www.repository.cam.ac.uk/handle/1810/319304 https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/f3ad2eba-e252-415b-b02e-945659c787b4/download e9af10ad30356802663f4eec35bca4ec https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/027c0597-b6e1-4c26-91f0-bc341b92b939/download 353adac0d1ebdfd65ab16480263c3c87 https://www.rioxx.net/licenses/all-rights-reserved/ Proteomics Cell biology DNA damage Subcellular localisation Pluripotency RBPs RNA Proteins LOPIT Post-transcriptional control