摘要
The reduction potential (E°′) is a critical parameter in determining the efficiency of most biological and chemical reactions. Biology employs three classes of metalloproteins to cover the majority of the 2-V range of physiological E°′s. An ultimate test of our understanding of E°′ is to find out the minimal number of proteins and their variants that can cover this entire range and the structural features responsible for the extreme E°′. We report herein the design of the protein azurin to cover a range from +970 mV to -954 mV vs. standard hydrogen electrode (SHE) by mutating only five residues and using two metal ions. Spectroscopic methods have revealed geometric parameters important for the high E°′. The knowledge gained and the resulting water-soluble redox agents with predictable E°′s, in the same scaffold with the same surface properties, will find wide applications in chemical, biochemical, biophysical, and biotechnological fields.
源语言 | 英语 |
---|---|
页(从-至) | 262-267 |
页数 | 6 |
期刊 | Proceedings of the National Academy of Sciences of the United States of America |
卷 | 113 |
期 | 2 |
DOI | |
出版状态 | 已出版 - 12 1月 2016 |
已对外发布 | 是 |