Biomineralization of a Cadmium Chloride Nanocrystal by a Designed Symmetrical Protein |
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Authors: | Dr Arnout R D Voet Hiroki Noguchi Dr Christine Addy Dr Kam Y J Zhang Prof Jeremy R H Tame |
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Affiliation: | 1. Structural Bioinformatics Team, Division of Structural and Synthetic Biology, Center for Life Science Technologies, RIKEN, 1‐7‐22, Suehiro, Tsurumi, Yokohama, 230‐0045 (Japan);2. Drug Design Laboratory, Yokohama City University, 1‐7‐29, Suehiro, Tsurumi, Yokohama, 230‐0045 (Japan) |
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Abstract: | We have engineered a metal‐binding site into the novel artificial β‐propeller protein Pizza. This new Pizza variant carries two nearly identical domains per polypeptide chain, and forms a trimer with three‐fold symmetry. The designed single metal ion binding site lies on the symmetry axis, bonding the trimer together. Two copies of the trimer associate in the presence of cadmium chloride in solution, and very high‐resolution X‐ray crystallographic analysis reveals a nanocrystal of cadmium chloride, sandwiched between two trimers of the protein. This nanocrystal, containing seven cadmium ions lying in a plane and twelve interspersed chloride ions, is the smallest reported to date. Our results indicate the feasibility of using rationally designed symmetrical proteins to biomineralize nanocrystals with useful properties. |
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Keywords: | biomineralization 2D crystals metalloproteins nanomaterials oligomers |
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