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Figure 4.15
Schematic for the assembly of multifunctionalized CCMV particles. Two
populations of particles are labeled and disassembled, and their subunits are purified.
The differentially labeled subunits are subsequently mixed together at different
ratios during re-assembly, resulting in multifunctional particles. Reproduced with
permission from Gillitzer, E., Suci, P., Young, M., and Douglas, T. (2006) Controlled
ligand display on a symmetrical protein-cage architecture through mixed assembly,
Small
,
2
(8-9), 962-966.
4.3.6 Atachment of Proteins and Nanomaterials 
Coupling strategies also allow the attachment of larger complexes such
as intact proteins, antibodies, or nanomaterials including quantum dots
(QDs), single-walled carbon nanotubes (SWCNTs), and fullerenes to VNPs
(Chatterji
et al.
, 2004b; Portney
et al.
, 2005; Sapsford
et al.
, 2006; Sen Gupta
et al.
, 2005a; Soto
et al.
, 2006; Steinmetz
et al.
, 2009b; Suci
et al.
, 2007a).
This can be achieved using homo- and heterobivalent chemical linkers and
covalent coupling; non-covalent strategies have also been explored (see
Section 4.3.8).
 
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