期刊
NATURE
卷 510, 期 7503, 页码 103-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature13404
关键词
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资金
- Howard Hughes Medical Institute
- JFRC
- National Science Foundation [CHE-1332907]
- International AIDS Vaccine Initiative, DTRA [N00024-10-D-6318/0024]
- AFOSR [FA950-12-10112]
- DOE [DE-SC0005155]
- NIH [T32GM067555]
- NSF [DGE-0718124]
- BER programme of the DOE Office of Science
- U.S. Department of Energy (DOE) [DE-SC0005155] Funding Source: U.S. Department of Energy (DOE)
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1332907] Funding Source: National Science Foundation
The self-assembly of proteins into highly ordered nanoscale architectures is a hallmark of biological systems. The sophisticated functions of these molecular machines have inspired the development of methods to engineer self-assembling protein nanostructures; however, the design of multi-component protein nanomaterials with high accuracy remains an outstanding challenge. Here we report a computational method for designing protein nanomaterials in which multiple copies of two distinct subunits co-assemble into a specific architecture. We use the method to design five 24-subunit cage-like protein nanomaterials in two distinct symmetric architectures and experimentally demonstrate that their structures are in close agreement with the computational design models. The accuracy of the method and the number and variety of two-component materials that it makes accessible suggest a route to the construction of functional protein nanomaterials tailored to specific applications.
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