| Literature DB >> 31050411 |
Zibo Chen, Matthew C Johnson, Jiajun Chen1, Matthew J Bick, Scott E Boyken, Baihan Lin, James J De Yoreo1, Justin M Kollman, David Baker, Frank DiMaio.
Abstract
Modular self-assembly of biomolecules in two dimensions (2D) is straightforward with DNA but has been difficult to realize with proteins, due to the lack of modular specificity similar to Watson-Crick base pairing. Here we describe a general approach to design 2D arrays using de novo designed pseudosymmetric protein building blocks. A homodimeric helical bundle was reconnected into a monomeric building block, and the surface was redesigned in Rosetta to enable self-assembly into a 2D array in the C12 layer symmetry group. Two out of ten designed arrays assembled to micrometer scale under negative stain electron microscopy, and displayed the designed lattice geometry with assembly size up to 100 nm under atomic force microscopy. The design of 2D arrays with pseudosymmetric building blocks is an important step toward the design of programmable protein self-assembly via pseudosymmetric patterning of orthogonal binding interfaces.Entities:
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Year: 2019 PMID: 31050411 PMCID: PMC7311176 DOI: 10.1021/jacs.9b01978
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419