| Literature DB >> 26631748 |
Parisa Hosseinzadeh1, Nicholas M Marshall2, Kelly N Chacón3, Yang Yu1, Mark J Nilges4, Siu Yee New1, Stoyan A Tashkov5, Ninian J Blackburn6, Yi Lu7.
Abstract
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.Entities:
Keywords: azurin; cupredoxins; electron transfer; reduction potential; secondary coordination sphere
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Year: 2015 PMID: 26631748 PMCID: PMC4720346 DOI: 10.1073/pnas.1515897112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205