Virus particles are probably the most precisely defined nanometre-sized objects that can be formed by protein self-assembly. Although their natural function is the storage and transport of genetic material, they have more recently been applied as scaffolds for mineralization and as containers for the encapsulation of inorganic compounds1,2. The reproductive power of viruses has been used to develop versatile analytical methods, such as phage display, for the selection and identification of (bio)active compounds3. To date, the combined use of self-assembly and reproduction has not been used for the construction of catalytic systems. Here we describe a self-assembled system based on a plant virus that has its coat protein genetically modified to provide it with a lipase enzyme. Using single-object and bulk catalytic studies, we prove that the virus-anchored lipase molecules are catalytically active. This anchored biocatalyst, unlike man-made supported catalysts, has the capability to reproduce itself in vivo, generating many independent catalytically active copies.
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The authors acknowledge the financial support provided through the European Community's Human Potential Programme under contract HPRN-CT-2001-00188 (SMASHYBIO). R.N. acknowledges financial support from the Royal Netherlands Academy of Sciences. We thank S. Chapman (Scottish Crop Research Institute, Invergowrie, Dundee, UK) for providing us with the pTXS.GFP-CP vector. We are indebted to H. Rogniaux for mass spectroscopy analysis.
The authors declare no competing financial interests.
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Carette, N., Engelkamp, H., Akpa, E. et al. A virus-based biocatalyst. Nature Nanotech 2, 226–229 (2007). https://doi.org/10.1038/nnano.2007.76
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