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Photo-uncaging of DEACM-CCP. The peptide was analyzed using <t>HPLC,</t> and the percentage of remaining CCP without uncaging is plotted against the photoirradiation time. The light doses 1 J/cm 2 corresponded to irradiation times of 10 s. Data represent the means ± S.D. of three independent experiments.
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Photo-uncaging of DEACM-CCP. The peptide was analyzed using <t>HPLC,</t> and the percentage of remaining CCP without uncaging is plotted against the photoirradiation time. The light doses 1 J/cm 2 corresponded to irradiation times of 10 s. Data represent the means ± S.D. of three independent experiments.
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Photo-uncaging of DEACM-CCP. The peptide was analyzed using <t>HPLC,</t> and the percentage of remaining CCP without uncaging is plotted against the photoirradiation time. The light doses 1 J/cm 2 corresponded to irradiation times of 10 s. Data represent the means ± S.D. of three independent experiments.
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Photo-uncaging of DEACM-CCP. The peptide was analyzed using HPLC, and the percentage of remaining CCP without uncaging is plotted against the photoirradiation time. The light doses 1 J/cm 2 corresponded to irradiation times of 10 s. Data represent the means ± S.D. of three independent experiments.

Journal: Scientific Reports

Article Title: Liquid–liquid phase separation by caged coacervating peptides

doi: 10.1038/s41598-026-40774-2

Figure Lengend Snippet: Photo-uncaging of DEACM-CCP. The peptide was analyzed using HPLC, and the percentage of remaining CCP without uncaging is plotted against the photoirradiation time. The light doses 1 J/cm 2 corresponded to irradiation times of 10 s. Data represent the means ± S.D. of three independent experiments.

Article Snippet: The solution was analyzed using a Chromaster HPLC instrument (Hitachi, Tokyo, Japan) with a C18 column (Symphonia C18, 4.6 × 150 mm; JASCO, Tokyo, Japan).

Techniques: Irradiation