The oxidative nuclease activity of human cytochrome c with mutations in Ω-loop C/D |
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| Institution: | 1. School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China;2. Hengyang Medical College, University of South China, Hengyang 421001, China;3. Key Lab of Protein Structure and Function of Universities in Hunan Province, University of South China, Hengyang 421001, China |
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| Abstract: | Natural and artificial nucleases have extensive applications in biotechnology and biomedicine. The exploration of protein with potential DNA cleavage activity also inspires the design of artificial nuclease and helps to understand the physiological process of DNA damage. In this study, we engineered four human cytochrome c (Cyt c) mutants (N52S, N52A, I81N, and I81D Cyt c), which showed enhanced DNA cleavage activity and degradation in comparison with WT Cyt c, especially under acidic conditions. The mechanism assays revealed that the superoxide (O2??) plays an important role in the nuclease reaction. The kinetic assays showed that the peroxidase activity of the I81D Cyt c mutant enhanced up to 9-fold at pH 5. This study suggests that the mutations of Ile81 and Asn52 in Ω-loop C/D are critical for the nuclease activity of Cyt c, which may have physiological significance in DNA damage and potential applications in biomedicine. |
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