4.5 Article

Hydration-Induced Structural Transitions in Biomimetic Tandem Repeat Proteins

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 125, Issue 8, Pages 2134-2145

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.0c11505

Keywords

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG) [SFB 1309-325871075]
  2. Center for NanoScience (CeNS)
  3. Fonds der Chemischen Industrie
  4. Universitatsgesellschaft Munchen
  5. United States Army Research Office [W911NF-16-1-0019, W911NF-18-1-026]
  6. Huck Endowment of The Pennsylvania State University

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A major challenge in developing biomimetic, high-performance, and sustainable products lies in accurately replicating the remarkable properties of biological materials, such as high strength, self-repair, and responsiveness to stimuli. State-of-the-art nuclear magnetic resonance (NMR) spectroscopy has been used to link the atomistic properties of an artificial bioinspired protein to its macroscopic properties, providing insights into the key factors behind its outstanding physical attributes. This in-depth characterization serves as a solid foundation for the development of advanced materials with enhanced properties.
A major challenge in developing biomimetic, high-performance, and sustainable products is the accurate replication of the biological materials' striking properties, such as high strength, self-repair, and stimuli-responsiveness. The rationalization of such features on the microscopic scale, together with the rational design of synthetic materials, is currently hindered by our limited understanding of the sequence-structure-property relationship. Here, employing state-of-the-art nuclear magnetic resonance (NMR) spectroscopy, we link the atomistic structural and dynamic properties of an artificial bioinspired tandem repeat protein TR(1,11) to its stunning macroscopic properties including high elasticity, self-healing capabilities, and record-holding proton conductivity among biological materials. We show that the hydration-induced structural rearrangement of the amorphous Gly-rich soft segment and the ordered Ala-rich hard segment is the key to the material's outstanding physical properties. We found that in the hydrated state both the Ala-rich ordered and Gly-rich disordered parts contribute to the formation of the nanoconfined beta-sheets, thereby enhancing the strength and toughness of the material. This restructuring is accompanied by fast proline ring puckering and backbone cis-trans isomerization at the water-protein interface, which in turn enhances the elasticity and the thermal conductivity of the hydrated films. Our in-depth characterization provides a solid ground for the development of next-generation materials with improved properties.

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