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Design of a Fe 4 S 4 cluster into the core of a de novo four‐helix bundle
Author(s) -
Mancini Joshua A.,
Pike Douglas H.,
Tyryshkin Alexei M.,
Haramaty Liti,
Wang Michael S.,
Poudel Saroj,
Hecht Michael,
Nanda Vikas
Publication year - 2020
Publication title -
biotechnology and applied biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 70
eISSN - 1470-8744
pISSN - 0885-4513
DOI - 10.1002/bab.2003
Subject(s) - helix bundle , cluster (spacecraft) , chemistry , cubane , crystallography , helix (gastropod) , sulfur , protein structure , stereochemistry , topology (electrical circuits) , combinatorial chemistry , biology , biochemistry , crystal structure , computer science , organic chemistry , ecology , mathematics , combinatorics , snail , programming language
We explore the capacity of the de novo protein, 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 in E. 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 functional de novo proteins with catalytic or electron‐transfer functionalities.