6IPP

Non-native ferritin 8-mer mutant-C90A/C102A/C130A/D144C

Summary for 6IPP

• Entry DOI: 10.2210/pdb6ipp/pdb
• Descriptor: Ferritin heavy chain, FE (III) ION (3 entities in total)
• Functional Keywords: ferritin, cysteine, oxidoreductase
• Biological source: Homo sapiens (Human)
• Total number of polymer chains: 2
• Total formula weight: 40747.01

Authors

Zang, J.,Chen, H.,Zhou, K.,Zhao, G. (deposition date: 2018-11-03, release date: 2019-03-13, Last modification date: 2023-11-22)

Primary citation

Zang, J.,Chen, H.,Zhang, X.,Zhang, C.,Guo, J.,Du, M.,Zhao, G.
Disulfide-mediated conversion of 8-mer bowl-like protein architecture into three different nanocages.
Nat Commun, 10:778-778, 2019

PubMed Abstract: Constructing different protein nanostructures with high-order discrete architectures by using one single building block remains a challenge. Here, we present a simple, effective disulfide-mediated approach to prepare a set of protein nanocages with different geometries from single building block. By genetically deleting an inherent intra-subunit disulfide bond, we can render the conversion of an 8-mer bowl-like protein architecture (NF-8) into a 24-mer ferritin-like nanocage in solution, while selective insertion of an inter-subunit disulfide bond into NF-8 triggers its conversion into a 16-mer lenticular nanocage. Deletion of the same intra-subunit disulfide bond and insertion of the inter-subunit disulfide bond results in the conversion of NF-8 into a 48-mer protein nanocage in solution. Thus, in the laboratory, simple mutation of one protein building block can generate three different protein nanocages in a manner that is highly reminiscent of natural pentamer building block originating from viral capsids that self-assemble into protein assemblies with different symmetries.

PubMed: 30770832
DOI: 10.1038/s41467-019-08788-9

Experimental method

X-RAY DIFFRACTION (2.699 Å)