TY - GEN AB - The goal of my PhD has been to develop and adapt optical chemical biology approaches to study signal transduction in cells. I developed genetically encoded FRET sensors to monitor with high temporal resolution PARP1-dependent ADP-ribosylation in live cells. I explored CB1 location-dependent functionality by adapting genetic code expansion to generate novel tagging strategies in live cells. Finally, I characterized chemically engineered lipid probes designed to follow lipid transport, metabolism and protein-interactions. AD - Oregon Health and Science University AU - Thomas, Alix DA - 2024-10-31 DO - 10.6083/bpxhc43998 DO - doi ID - 43998 KW - Signal Transduction KW - Fluorescence Resonance Energy Transfer KW - ADP-Ribosylation KW - Lipids KW - Receptor, Cannabinoid, CB1 KW - chemical biology KW - FRET KW - ADPr KW - CB1 L1 - https://digitalcollections.ohsu.edu/record/43998/files/Thomas.Alix.2024.pdf L2 - https://digitalcollections.ohsu.edu/record/43998/files/Thomas.Alix.2024.pdf L4 - https://digitalcollections.ohsu.edu/record/43998/files/Thomas.Alix.2024.pdf LA - eng LK - https://digitalcollections.ohsu.edu/record/43998/files/Thomas.Alix.2024.pdf N2 - The goal of my PhD has been to develop and adapt optical chemical biology approaches to study signal transduction in cells. I developed genetically encoded FRET sensors to monitor with high temporal resolution PARP1-dependent ADP-ribosylation in live cells. I explored CB1 location-dependent functionality by adapting genetic code expansion to generate novel tagging strategies in live cells. Finally, I characterized chemically engineered lipid probes designed to follow lipid transport, metabolism and protein-interactions. PB - Oregon Health and Science University PY - 2024-10-31 T1 - Development of chemical biology tools to follow signal transduction in cells TI - Development of chemical biology tools to follow signal transduction in cells UR - https://digitalcollections.ohsu.edu/record/43998/files/Thomas.Alix.2024.pdf Y1 - 2024-10-31 ER -