4.8 Article

Spatially Patterned, Porous Protein Crystals as Multifunctional Materials

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.3c06348

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The use of protein crystals as functional materials can be enhanced through spatial patterning and morphology control, enabling them to act as reaction vessels for complex multi-step reactions and broadening their utility as solid-state materials. The examples presented here demonstrate the generation of patterned, multi-enzyme frameworks with cooperative catalytic behavior and Janus-type architectures with anisotropic arrangement of chemically distinct domains, showcasing the potential of protein crystals in materials science and nanotechnology.
While the primary use of protein crystals has historically been in crystallographic structure determination, they have recently emerged as promising materials with many advantageous properties such as high porosity, biocompatibility, stability, structural and functional versatility, and genetic/chemical tailorability. Here, we report that the utility of protein crystals as functional materials can be further augmented through their spatial patterning and control of their morphologies. To this end, we took advantage of the chemically and kinetically controllable nature of ferritin self-assembly and constructed core-shell crystals with chemically distinct domains, tunable structural patterns, and morphologies. The spatial organization within ferritin crystals enabled the generation of patterned, multi-enzyme frameworks with cooperative catalytic behavior. We further exploited the differential growth kinetics of ferritin crystal facets to assemble Janus-type architectures with an anisotropic arrangement of chemically distinct domains. These examples represent a step toward using protein crystals as reaction vessels for complex multi-step reactions and broadening their utility as functional, solid-state materials. Our results demonstrate that morphology control and spatial patterning, which are key concepts in materials science and nanotechnology, can also be applied for engineering protein crystals.

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