Abstract
The cowpea chlorotic mottle virus (CCMV) is a nanoparticle that holds promise for diagnostic and therapeutic applications. The empty virus-like particle, however, is not stable under physiological conditions. Here, we describe a systematic study into the expansion of the assembly properties of a protein based block copolymer of the CCMV capsid protein and an elastin-like polypeptide. By systematically changing the hydrophobicity of the stimulus-responsive elastin-like polypeptide block, assembly of the capsid proteins could be achieved at close to physiological conditions. This strategy may prove to be useful in the development of a physiologically stable CCMV capsid variant. (C) 2017 Elsevier Ltd. All rights reserved.
| Original language | English |
|---|---|
| Article number | 33 |
| Pages (from-to) | 4968-4971 |
| Number of pages | 4 |
| Journal | Tetrahedron |
| Volume | 73 |
| Issue number | 33 |
| DOIs | |
| Publication status | Published - 17 Aug 2017 |
Keywords
- Cowpea chlorotic mottle virus
- Elastin-like polypeptide
- Self-assembly
- Viral capsid
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