Protein-directed self-assembly of a fullerene crystal
Document Type
Article
Publication Date
4-26-2016
Abstract
Learning to engineer self-assembly would enable the precise organization of molecules by design to create matter with tailored properties. Here we demonstrate that proteins can direct the self-assembly of buckminsterfullerene (C 60) into ordered superstructures. A previously engineered tetrameric helical bundle binds C 60 in solution, rendering it water soluble. Two tetramers associate with one C 60, promoting further organization revealed in a 1.67-Å crystal structure. Fullerene groups occupy periodic lattice sites, sandwiched between two Tyr residues from adjacent tetramers. Strikingly, the assembly exhibits high charge conductance, whereas both the protein-alone crystal and amorphous C 60 are electrically insulating. The affinity of C 60 for its crystal-binding site is estimated to be in the nanomolar range, with lattices of known protein crystals geometrically compatible with incorporating the motif. Taken together, these findings suggest a new means of organizing fullerene molecules into a rich variety of lattices to generate new properties by design.
Identifier
84964978092 (Scopus)
Publication Title
Nature Communications
External Full Text Location
https://doi.org/10.1038/ncomms11429
e-ISSN
20411723
PubMed ID
27113637
Volume
7
Grant
CHE-1413295
Fund Ref
National Institutes of Health
Recommended Citation
Kim, Kook Han; Ko, Dong Kyun; Kim, Yong Tae; Kim, Nam Hyeong; Paul, Jaydeep; Zhang, Shao Qing; Murray, Christopher B.; Acharya, Rudresh; Degrado, William F.; Kim, Yong Ho; and Grigoryan, Gevorg, "Protein-directed self-assembly of a fullerene crystal" (2016). Faculty Publications. 10573.
https://digitalcommons.njit.edu/fac_pubs/10573
