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Complete and cooperative in vitro assembly of computationally designed self-assembling protein nanomaterials

Adam J. Wargacki, Tobias P. Wörner, Michiel Waterbeemd, Daniel Ellis, Albert J. R. Heck and Neil P. King ()
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Adam J. Wargacki: University of Washington
Tobias P. Wörner: Utrecht University
Michiel Waterbeemd: Utrecht University
Daniel Ellis: University of Washington
Albert J. R. Heck: Utrecht University
Neil P. King: University of Washington

Nature Communications, 2021, vol. 12, issue 1, 1-14

Abstract: Abstract Recent advances in computational methods have enabled the predictive design of self-assembling protein nanomaterials with atomic-level accuracy. These design strategies focus exclusively on a single target structure, without consideration of the mechanism or dynamics of assembly. However, understanding the assembly process, and in particular its robustness to perturbation, will be critical for translating this class of materials into useful technologies. Here we investigate the assembly of two computationally designed, 120-subunit icosahedral complexes in detail using several complementary biochemical methods. We found that assembly of each material from its two constituent protein building blocks was highly cooperative and yielded exclusively complete, 120-subunit complexes except in one non-stoichiometric regime for one of the materials. Our results suggest that in vitro assembly provides a robust and controllable route for the manufacture of designed protein nanomaterials and confirm that cooperative assembly can be an intrinsic, rather than evolved, feature of hierarchically structured protein complexes.

Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21251-y

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DOI: 10.1038/s41467-021-21251-y

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