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Fabrication of functional nanostructures is a prominent issue in nanotechnology, because they often exhibit unique properties that are different from the individual building blocks. Protein cage nanoparticles are attractive nanobuilding blocks for constructing nanostructures due to their well-defined symmetric spherical structures, polyvalent nature, and functional plasticity. Here, a lumazine synthase protein cage nanoparticle is genetically modified to be used as a template to generate functional nanobuilding blocks and covalently display enzymes (β-lactamase) and protein ligands (FKBP12/FRB) on its surface, making dual-functional nanobuilding blocks. Nanoreaction clusters are subsequently created by ligand-mediated alternate deposition of two complementary building blocks using layer-by-layer (LbL) assemblies. 3D nanoreaction clusters provide enhanced enzymatic activity compared with monolayered building block arrays. The approaches described here may provide new opportunities for fabricating functional nanostructures and nanoreaction clusters, leading to the development of new protein nanoparticle-based nanostructured biosensor devices.
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http://dx.doi.org/10.1002/smll.201801488 | DOI Listing |
Small
September 2024
School of Chemistry, Dalian University of Technology, Dalian, 116024, China.
Small
August 2018
Department of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.
Langmuir
October 2010
Department III, Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
We give a detailed confocal fluorescence microscopy study on reverse vesicles from a salt-free catanionic surfactant system. When tetradecyltrimethylammonium laurate (TTAL) and lauric acid (LA) are mixed in cyclohexane at the presence of a small amount of water, stable reverse vesicular phases form spontaneously. The reverse vesicular phases can be easily labeled with dyes of varying molecular size and hydrophobicity while the dyes are nearly insoluble in cyclohexane without reverse vesicles.
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