4.8 Article

DNA-Functionalized, Bivalent Proteins

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 22, Pages 6776-6779

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b03403

Keywords

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Funding

  1. Vannevar Bush Faculty Fellowship program - Basic Research Office of the Assistant Secretary of Defense for Research and Engineering
  2. Office of Naval Research [N00014-15-1-0043]
  3. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF ECCS-1542205]
  4. MRSEC program at the Materials Research Center [NSF DMR-1121262]
  5. Keck Foundation
  6. State of Illinois, through the International Institute for Nanotechnology
  7. National Science and Engineering Research Council of Canada

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Bivalent DNA conjugates of beta-galactosidase (beta Gal), having pairs of oligonucleotides positioned closely on opposing faces of the protein, have been synthesized and characterized. These structures, due to their directional bonding characteristics, allow for the programmable access of one-dimensional protein materials. When conjugates functionalized with complementary oligonucleotides are combined under conditions that support DNA hybridization, periodic wire-type superstructures consisting of aligned proteins form. These structures have been characterized by gel electrophoresis, cryo-transmission electron microscopy, and negative-stain transmission electron microscopy. Significantly, melting experiments of complementary building blocks display narrowed and elevated melting transitions compared to the free duplex DNA, further supporting the formation of the designed binding mode, and unambiguously characterizing their association as DNA-mediated. These novel structures illustrate, for the first time, that directional DNA bonding can be realized with only a pair of DNA modifications, which will allow one to engineer directional interactions and realize new classes of superstructures not possible simply through shape control or isotropically functionalized materials.

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