| Literature DB >> 18318461 |
Erica Strable1, Duane E Prasuhn, Andrew K Udit, Steven Brown, A James Link, John T Ngo, Gabriel Lander, Joel Quispe, Clinton S Potter, Bridget Carragher, David A Tirrell, M G Finn.
Abstract
Virus-like particles composed of hepatitis B virus (HBV) or bacteriophage Qbeta capsid proteins have been labeled with azide- or alkyne-containing unnatural amino acids by expression in a methionine auxotrophic strain of E. coli. The substitution does not affect the ability of the particles to self-assemble into icosahedral structures indistinguishable from native forms. The azide and alkyne groups were addressed by Cu(I)-catalyzed [3 + 2] cycloaddition: HBV particles were decomposed by the formation of more than 120 triazole linkages per capsid in a location-dependent manner, whereas Qbeta suffered no such instability. The marriage of these well-known techniques of sense-codon reassignment and bioorthogonal chemical coupling provides the capability to construct polyvalent particles displaying a wide variety of functional groups with near-perfect control of spacing.Entities:
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Year: 2008 PMID: 18318461 PMCID: PMC2713011 DOI: 10.1021/bc700390r
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774