4.8 Article

Regulation of the Inevitable Water-Responsivity of Silk Fibroin Biopolymer by Polar Amino Acid Activation

Journal

ACS NANO
Volume 16, Issue 10, Pages 17274-17288

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c07971

Keywords

silk fibroin; amino acid; water diffusion; hydration-adaptive crystallization; tissue adhesive

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [NRF-2017R1E1A1A01074343]
  2. Korea Medical Device Development Fund - Korea government (the Ministry of Science and ICT)
  3. Ministry of Trade, Industry and Energy
  4. Ministry of Health & Welfare, Republic of Korea
  5. Ministry of Food and Drug Safety [202011D04]
  6. Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Ministry of Science ICT [2019M3A9H1103786]
  7. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2021R1A4A3030268]
  8. National Research Foundation of Korea [2019M3A9H1103786] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Water-responsive crystallization is a typical behavior of biopolymers, which has implications for the development of intelligent human-robot interfaces. However, it also hinders the consistent adhesion of tissue adhesive. This study developed an amino acid-based technology to regulate the crystallization of silk fibroin, achieving targeted control over the crystallization process.
In nature, water is vital for maintaining homeostasis. Particularly, organisms (e.g., plant leaf, bird feather) exploit water fluidics for motions. Hydration-adaptive crystallization is the representative water-responsive actuation of biopolymers. This crystallization has inspired the development of intelligent human-robot interfaces. At the same time, it hinders the consistent adhesion of tissue adhesive. As hydration-adaptive crystallization is inevitable, the on-demand control of crystallization is desirable in the innovative biopolymeric biomedical systems. To this end, this study developed an amino acid-based technology to artificially up- or down-regulate the inevitable crystallization of silk fibroin. A case II diffusion model was constructed, and it revealed that the activity of polar amino acid is related to crystallization kinetics. Furthermore, the water dynamics study suggested that active amino acid stabilizes crystallization-triggering water molecules. As a proof-of-concept, we verified that a 30% increase in the activity of serine resulted in a 50% decrease in the crystallization rate. Furthermore, the active amino acid-based suppression of hydration-adaptive crystallization enabled the silk fibroin to keep its robust adhesion (approximately 160 kJ m(-3)) by reducing the water-induced loss of adhesive force. The proposed silk fibroin was demonstrated as a stable tissue adhesive applied on ex vivo porcine mandible tissue. This amino acid-based regulation of hydration-adaptive crystallization will pioneer next-generation biopolymer-based healthcare.

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