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• W4242940063 abstract "Protein degradation is a regulatory process essential to cell viability and its dysfunction is implicated in many diseases, such as aging and neurodegeneration. In this report, stimulated Raman scattering microscopy coupled with metabolic labeling with 13C-phenylalanine is used to visualize protein degradation in living cells with subcellular resolution. We choose the ring breathing modes of endogenous 12C-phenylalanine and incorporated 13C-phenylalanine as protein markers for the original and nascent proteomes, respectively, and the decay of the former wasquantified through 12C/(12C+13C) ratio maps. We demonstrate time-dependent imaging of proteomic degradation in mammalian cells under steady-state conditions and various perturbations, including oxidative stress, cell differentiation, and huntingtin protein aggregation." @default.
• W4242940063 created "2022-05-12" @default.
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• W4242940063 date "2014-04-15" @default.
• W4242940063 modified "2023-10-16" @default.
• W4242940063 title "Live-Cell Quantitative Imaging of Proteome Degradation by Stimulated Raman Scattering" @default.
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• W4242940063 doi "https://doi.org/10.1002/ange.201310725" @default.
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