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. 2017 Jul 26;7:6513. doi: 10.1038/s41598-017-06872-y

Figure 5.

Figure 5

Curcumin and Curcuma longa L. extract regulate the formation of disulfide bonds during oxidative protein folding. (a) Liver lysates were analyzed for the presence of PDI in high-molecular-weight complexes using non-reducing gels. (b) Liver lysates were derivatized with DNPH, electrophoresed under non-reducing conditions, and immunoblotted with anti-DNP antibody. Independently, liver samples were immunoprecipitated and immunoblotted with anti-PDI antibody in reducing gel condition and immunoblotted with anti-PDI antibody. (c) PDI-reductase activity was measured in the same-treated liver samples. Results are presented as percentages of the PDI activity of control rats. (d) Liver lysates were immunoprecipitated with anti-PDI or anti-apoB antibody and immunoblotted with anti-apoB or anti-PDI antibody, respectively. (e) Oxygen-consumption kinetics were assayed using isolated ER fractions from 1 day and 4 week CCl4-treated rats. The experiments were carried out three times with similar activity profiles. The experiments were repeated three times using tissue from at least three different rats. CL: Curcuma longa L., PDI: protein disulfide isomerase, DNPH: 2,4-dinitrophenylhydrazine, DNP: dinitrophenol.