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- W4213433896 abstract "The small biomolecule methionine (Met) is a fundamental amino acid required for a vast range of biological processes such as protein synthesis, cancer metabolism, and epigenetics. However, it is still difficult to visualize the subcellular distribution of small biomolecules including Met in a minimally invasive manner. Here, we demonstrate stimulated Raman scattering (SRS) imaging of cellular uptake of deuterated methionine (d8-Met) in live HeLa cells by way of comparison to the previously used alkyne-labeled Met analogue─homopropargylglycine (Hpg). We show that the solutions of d8-Met and Hpg have similar SRS signal intensities. Furthermore, by careful image analysis with background subtraction, we succeed in the SRS imaging of cellular uptake of d8-Met with a much greater signal intensity than Hpg, possibly reflecting the increased and minimally invasive uptake kinetics of d8-Met compared with Hpg. We anticipate that d8-Met and other deuterated biomolecules will be useful for investigating metabolic processes with subcellular resolution." @default.
- W4213433896 created "2022-02-25" @default.
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- W4213433896 date "2022-02-23" @default.
- W4213433896 modified "2023-10-09" @default.
- W4213433896 title "Probing Methionine Uptake in Live Cells by Deuterium Labeling and Stimulated Raman Scattering" @default.
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- W4213433896 doi "https://doi.org/10.1021/acs.jpcb.1c08343" @default.
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