Abstract
Human immunodeficiency virus type 1 subtype B and C proteases were manipulated to contain 90M, 88D, or 89L, and their in vitro biological properties were studied. We showed that D30N has significantly more impact in subtype C than in subtype B counterparts, accounting for the reported low prevalence of this mutation in patients failing nelfinavir-based regimens.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Cell Line
-
Cloning, Molecular
-
DNA Primers
-
Drug Resistance, Viral
-
HIV Infections / virology
-
HIV Protease / genetics*
-
HIV Protease Inhibitors / pharmacology*
-
HIV-1 / drug effects*
-
HIV-1 / enzymology*
-
HIV-1 / genetics
-
Humans
-
Isoenzymes / genetics
-
Mutation / genetics*
-
Nelfinavir / pharmacology*
-
Phenotype
-
RNA, Viral / genetics
-
Recombinant Fusion Proteins / genetics
-
Reverse Transcriptase Polymerase Chain Reaction
-
Transfection
-
Virus Replication / drug effects
Substances
-
DNA Primers
-
HIV Protease Inhibitors
-
Isoenzymes
-
RNA, Viral
-
Recombinant Fusion Proteins
-
HIV Protease
-
Nelfinavir