4.6 Article

Ca2+-induced self-assembly of Bombyx mori silk sericin into a nanofibrous network-like protein matrix for directing controlled nucleation of hydroxylapatite nano-needles

期刊

JOURNAL OF MATERIALS CHEMISTRY B
卷 3, 期 12, 页码 2455-2462

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4tb01944j

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资金

  1. Zhejiang Provincial Natural Science Foundation of China [LZ12C17001]
  2. Projects of Zhejiang Provincial Science and Technology Plans [2012C12910]
  3. National Natural Science Foundation of China [21172194]
  4. Silkworm Industry Science and Technology Innovation Team [2011R50028]
  5. National High Technology Research and Development Program 863 [2013AA102507]
  6. National Science Foundation [DMR-0847758, CMMI-1234957, CBET-0854414]
  7. Department of Defense Peer Reviewed Medical Research Program [W81XWH-12-1-0384]
  8. Oklahoma Center for Adult Stem Cell Research [434003]
  9. Oklahoma Center for the Advancement of Science and Technology [HR14-160]
  10. National Institutes of Health [EB015190]
  11. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R21EB015190] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Bone biomineralization is a well-regulated protein-mediated process where hydroxylapatite (HAP) crystals are nucleated with preferred orientation within the self-assembled protein matrix. Mimicking this process is a promising approach to the production of bone-like protein/mineral nanocomposites for bone repair and regeneration. Towards the goal of fabricating such nanocomposites from sericin, a protein spun by Bombyx mori (B. mori) silkworm, and bone mineral HAP, for the first time we investigated the chemical mechanism underpinning the synergistic processes of the conformational change/self-assembly of B. mori sericin (BS) as well as the nucleation of HAP on the resultant self-assembled BS matrix. We found that BS, rich in anionic amino acid residues, could bind Ca2+ ions from the HAP precursor solution through electrostatic attraction. The Ca2+ binding drove the conformational change of BS from random coils into beta-sheets and its concomitant self-assembly into the interconnected nanofibrous network-like protein matrix, which initiated the nucleation and growth of HAP crystals. HAP crystals directed by the resultant self-assembled BS matrix grew preferentially along their crystallographic c-axis, leading to the formation of HAP nano-needles. The HAP nano-needles in the self-assembled BS matrix were subsequently aggregated into globules, probably driven by the hydrogen bonding between C=O groups of BS and O-H groups of HAP nano-needles. The present work sheds light on the chemical mechanisms of BS self-assembly and the controlled mineralization directed by the self-assembled matrix. We also found that the resultant nanocomposites could promote the osteogenic differentiation of human bone marrow-derived mesenchymal stem cells. Thus our work also generates a biomimetic approach to bone-like silk protein/mineral nanocomposite scaffolds that can find potential applications in bone repair and regeneration.

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