Affiliation:
1. Beijing Key Laboratory of Lignocellulosic Chemistry MOE Engineering Research Center of Forestry Biomass Materials and Energy Beijing Forestry University Beijing 100083 China
2. China National Pulp and Paper Research Institute Beijing 100102 China
3. State Key Laboratory of Efficient Production of Forest Resources Beijing 100083 China
Abstract
AbstractDespite the first observations that the perforin can punch holes in target cells for live/dead cycles in the human immune system over 110 years ago, emulating this behavior in materials science remains challenging. Here, a perforin‐mimicking molecular drilling strategy is employed to engineer macroporous hollow lignin spheres as performance‐configurable catalysts, adhesives, and gels. Using a toolbox of over 20 molecular compounds, the local curvature of amphiphilic lignin is modulated to generate macroporous spheres with hole sizes ranging from 0 to 100 nm. Multiscale control is precisely achieved through noncovalent assembly directing catalysis, synthesis, and polymerization. Exceptional performance mutations correlate with the changes in hole size, including an increase in catalytic efficiency from 50% to 100%, transition from nonstick synthetics to ultrastrong adhesives (adhesion ≈18.3 MPa, exceeding that of classic epoxies), and transformation of viscous sols to tough nanogels. Thus, this study provides a robust and versatile noncovalent route for mimicking perforin‐induced structural variations in cells, representing a significant stride toward the exquisite orchestration of assemblies over multiple length scales.
Funder
Fundamental Research Funds for the Central Universities
National Science Fund for Distinguished Young Scholars
National Natural Science Foundation of China
Higher Education Discipline Innovation Project
Cited by
8 articles.
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