Abstract
A new strategy is described for the modification of CCMV for loading of cargoes inside the viral capsid. Sortase A, an enzyme which is present in Gram-positive bacteria, was used to attach cargo to the glycine-tagged N-termini of several CCMV variants. We show that small molecules and proteins bearing a C-terminal LPETG-motif can be attached in this way. This method allows for the site-specific, covalent, and orthogonal modification of CCMV capsids in a mild fashion, leading to high encapsulation efficiencies. This strategy can easily be expanded to other types of cargoes, labeled with an LPETG-tag without altering protein function.
| Original language | English |
|---|---|
| Pages (from-to) | 2429-2434 |
| Number of pages | 6 |
| Journal | Bioconjugate Chemistry |
| Volume | 26 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 16 Dec 2015 |
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