Source:http://linkedlifedata.com/resource/pubmed/id/10662613
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2000-3-8
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pubmed:abstractText |
Ribozymes are catalytic RNAs that offer several advantages as specific therapeutic genes against human immunodeficiency virus type 1 (HIV-1). Significant challenges in antiviral uses of ribozymes include (1) how best to express and to deliver this agent and (2) what is the best locale to target ribozymes against HIV-1 RNA. To explore the former, we have previously characterized several vector systems for efficient expression/delivery of anti-HIV-1 ribozymes (Dropulic et al., 1992; Dropulic and Jeang, 1994a; Smith et al., 1997). Here, to investigate an optimal locale for ribozyme-targeting, we asked whether it might be advantageous to direct ribozymes into HIV-1 virions as opposed to the more conventional approach of targeting ribozymes into infected cells. Two series of experiments were performed. First, we demonstrated that anti-HIV-1 ribozymes could indeed be packaged specifically and efficiently into virions. Second, we compared the virus suppressing activity of a packageable ribozyme with its counterpart, which cannot be packaged into HIV-1 virions. Our results showed that although both ribozymes cleaved HIV-1 genomic RNA in vitro with equivalent efficiencies, the former ribozyme demonstrated significantly higher virus-suppressing activity than the latter. These findings provide proof-of-principle that to combat productive HIV-1 replication, intravirion targeting is more effective than intracellular targeting of ribozymes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0042-6822
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2000 Academic Press.
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
267
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
174-84
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10662613-Base Sequence,
pubmed-meshheading:10662613-Cell Line,
pubmed-meshheading:10662613-Gene Products, pol,
pubmed-meshheading:10662613-Gene Targeting,
pubmed-meshheading:10662613-HIV,
pubmed-meshheading:10662613-HeLa Cells,
pubmed-meshheading:10662613-Humans,
pubmed-meshheading:10662613-Hydrolysis,
pubmed-meshheading:10662613-RNA, Catalytic,
pubmed-meshheading:10662613-RNA, Viral,
pubmed-meshheading:10662613-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:10662613-Virion,
pubmed-meshheading:10662613-Virus Assembly
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pubmed:year |
2000
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pubmed:articleTitle |
Intravirion targeting of a functional anti-human immunodeficiency virus ribozyme directed to pol.
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pubmed:affiliation |
Molecular Virology Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, 9000 Rockville Pike, Bethesda, Maryland 20892-0460, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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