| Literature DB >> 24318884 |
Robert J Scarborough1, Michel V Lévesque, Jean-Pierre Perreault, Anne Gatignol.
Abstract
Nucleic acid therapies targeting HIV replication have the potential to be used in conjunction with or in place of the standard small-molecule therapies. Among the different classes of nucleic acid therapies, several ribozymes (Rzs, RNA enzymes) have been developed to target HIV RNA. The design of Rzs targeting HIV RNA is complicated by the sequence diversity of viral strains and the structural diversity of their target sites. Using the SOFA-HDV Rz as an example, this chapter describes methods that can be used to design Rzs for controlling HIV replication. We describe how to (1) identify highly conserved Rz target sites in HIV RNA; (2) generate a set of Rzs with the potential to be used as therapeutics; and (3) screen these Rzs for activity against HIV production.Mesh:
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Year: 2014 PMID: 24318884 DOI: 10.1007/978-1-62703-730-3_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745