期刊
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY
卷 67, 期 4, 页码 574-585出版社
WILEY
DOI: 10.1002/bab.2003
关键词
de novoprotein; iron-sulfur cluster; combinatorial library; protein design; electron transfer; oxidoreductase
资金
- NASA Astrobiology Grant [80NSSC18M0093]
- NASA postdoctoral fellowship
We explore the capacity of thede novoprotein, S824, to incorporate a multinuclear iron-sulfur cluster within the core of a single-chain four-helix bundle. This topology has a high intrinsic designability because sequences are constrained largely by the pattern of hydrophobic and hydrophilic amino acids, thereby allowing for the extensive substitution of individual side chains. Libraries of novel proteins based on these constraints have surprising functional potential and have been shown to complement the deletion of essential genes inE. coli. Our structure-based design of four first-shell cysteine ligands, one per helix, in S824 resulted in successful incorporation of a cubane Fe(4)S(4)cluster into the protein core. A number of challenges were encountered during the design and characterization process, including nonspecific metal-induced aggregation and the presence of competing metal-cluster stoichiometries. The introduction of buried iron-sulfur clusters into the helical bundle is an initial step toward converting libraries of designed structures into functionalde novoproteins with catalytic or electron-transfer functionalities.
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