Peptide Inhibitor of Complement C1 (PIC1) demonstrates antioxidant activity via single electron transport (SET) and hydrogen atom transfer (HAT)

• Published in: PloS one 2018-03, Vol.13 (3), p.e0193931
• Main Authors: Gregory Rivera, Magdielis, Hair, Pamela S, Cunnion, Kenji M, Krishna, Neel K
• Format: Article
• Language: English
• Subjects: Antioxidants; Assaying; Biology; Biology and Life Sciences; Blood plasma; Byproducts; Chelation; Complement; Complement component C1; Copper; Cysteine; Disease; Electron transport; Free radicals; Glutathione; Hair; Heme; Hemoglobin; Hydrogen; Hydrogen atoms; Hydrogen ion concentration; Hydroxyl radicals; Inhibitors; Kidneys; Lipids; Medical schools; Medicine and Health Sciences; Methods; Myoglobin; Myoglobins; Organs; Oxidation; Oxidative stress; Oxygen; Pediatrics; Peptide inhibitors; Peptides; Peroxidase; Physical Sciences; Proteins; Reactive oxygen species; Residues; Rodents; Thiobarbituric acid; Tissues; Uric acid
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0193931

Reactive oxygen species (ROS) are natural byproducts of oxidative respiration that are toxic to organs and tissues. To mitigate ROS damage, organisms have evolved a variety of antioxidant systems to counteract these harmful molecules, however in certain pathological conditions these protective mechanisms can be overwhelmed. We have recently demonstrated that Peptide Inhibitor of Complement C1 (PIC1) mitigates peroxidase activity of the heme bearing proteins myeloperoxidase, hemoglobin, and myoglobin through a reversible process. To determine if this property of PIC1 was antioxidant in nature, we tested PIC1 in a number of well-established antioxidant assays. PIC1 showed dose-dependent antioxidant activity in a total antioxidant (TAC) assay, hydroxyl radical antioxidant capacity (HORAC) assay, oxygen radical antioxidant capacity (ORAC) assay as well as the thiobarbituric acid reactive substances (TBARS) assay to screen for PIC1 antioxidant activity in human plasma. The antioxidant activity of PIC1 in the TAC assay, as well as the HORAC/ORAC assay demonstrated that this peptide acts via the single electron transport (SET) and hydrogen atom transfer (HAT) mechanisms, respectively. Consistent with this mechanism of action, PIC1 did not show activity in a metal chelating activity (MCA) assay. PIC1 contains two vicinal cysteine residues and displayed similar antioxidant activity to the well characterized cysteine-containing tripeptide antioxidant molecule glutathione (GSH). Consistent with the role of the cysteine residues in the antioxidant activity of PIC1, oxidation of these residues significantly abrogated antioxidant activity. These results demonstrate that in addition to its described complement inhibiting activity, PIC1 displays in vitro antioxidant activity.