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. 2020 Sep 10;11:4530. doi: 10.1038/s41467-020-17595-6

Fig. 3. Characterization of intracellular reduction of ionic gold.

Fig. 3

Raman spectra (a) of cells treated with either ionic Au–PEG clusters after 240 min (burgundy), 120 min (red), 60 min (orange), 30 min (yellow), Au3+ (green), or Na–PEG (blue). Raman mapping (of 2800–3000 peak intensity) with the corresponding bright field and merged images for 240 min treatments of Au–PEG, Au3+ and Na–PEG (b). Scale bars for (b) are 20 µm. c Raman spectra of Au–PEG-treated MCF-7 cellular fractions separated using differential centrifugation including the nucleus and large organelles, 15,000 g (red); mitochondria, lysosomes and other medium sized organelles, 100,000 g (green); membrane fragments, 300,000 g (blue); and highly soluble/cytosolic molecules (violet), >300,000 g; and the glass slide without cell fractions (black). d SDS-PAGE stained with Coomassie Blue with intensity plots overlaid of protein from the nuclear fraction of MCF-7 cells without treatment (green), treated with Na–PEG (blue), or Au–PEG (yellow) with standard SDS-PAGE conditions (lighter-shaded colors, left three lanes), or without β-mercaptoethanol (darker-shaded colors, right three lanes).