Self-assembly and modular functionalization of three-dimensional crystals from oppositely charged proteins

Multicomponent crystals and nanoparticle superlattices are a powerful approach to integrate different materials into ordered nanostructures. Well-developed, especially DNA-based, methods for their preparation exist, yet most techniques concentrate on molecular and synthetic nanoparticle systems in n...

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Veröffentlicht in:Nature communications 2014-07, Vol.5 (1), p.4445, Article 4445
Hauptverfasser: Liljeström, Ville, Mikkilä, Joona, Kostiainen, Mauri A.
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Sprache:eng
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Zusammenfassung:Multicomponent crystals and nanoparticle superlattices are a powerful approach to integrate different materials into ordered nanostructures. Well-developed, especially DNA-based, methods for their preparation exist, yet most techniques concentrate on molecular and synthetic nanoparticle systems in non-biocompatible environment. Here we describe the self-assembly and characterization of binary solids that consist of crystalline arrays of native biomacromolecules. We electrostatically assembled cowpea chlorotic mottle virus particles and avidin proteins into heterogeneous crystals, where the virus particles adopt a non-close-packed body-centred cubic arrangement held together by avidin. Importantly, the whole preparation process takes place at room temperature in a mild aqueous medium allowing the processing of delicate biological building blocks into ordered structures with lattice constants in the nanometre range. Furthermore, the use of avidin–biotin interaction allows highly selective pre- or post-functionalization of the protein crystals in a modular way with different types of functional units, such as fluorescent dyes, enzymes and plasmonic nanoparticles. Multicomponent crystals are promising structures for the design of nanomaterials with adjustable properties. Here, the authors present a novel strategy for the construction of binary crystals consisting of oppositely charged biomacromolecule building blocks.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms5445