Population
Cells infected with mutant positive-strand RNA virus
Comparison
Introduction of catalytically inactive… vs Active polymerases
Design
Preclinical
Authors
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Animal data suggest multimer interfaces as antiviral targets; leaves open translation to human RNA virus therapies.
Targeting the multimeric arrays of RNA-dependent RNA polymerase, rather than just the active sites, may provide a novel and more effective antiviral strategy.
Spagnolo et al. (2010) studied this question.
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