Comparison of raltegravir and elvitegravir on HIV-1 integrase catalytic reactions and on a series of drug-resistant integrase mutants.

Methods Development
Therapeutic Approaches


HIV-1 integrase (IN) is the molecular target of the newly approved anti-AIDS drug raltegravir (MK-0518, Isentress) while elvitegravir (GS-9137, JTK-303) is in clinical trials. The aims of the present study were (1) to investigate and compare the effects of raltegravir and elvitegravir on the three IN-mediated reactions, 3'-processing (3'-P), strand transfer (ST), and disintegration, (2) to determine the biochemical activities of seven IN mutants (T66I, L74M, E92Q, F121Y, Q148K, S153Y, and N155H) previously selected from drug-resistant patients and isolates, and (3) to determine the resistance profile for raltegravir and elvitegravir in those IN mutants. Our findings demonstrate that both raltegravir and elvitegravir are potent IN inhibitors and are highly selective for the ST reaction of IN. Elvitegravir was more potent than raltegravir, but neither drug could block disintegration. All resistance mutations were at least partially impaired for ST. Q148K was also markedly impaired for 3'-P. Both drugs exhibited a parallel resistance profile, although resistance was generally greater for elvitegravir. Q148K and T66I conferred the highest resistance to both drugs while S153Y conferred relatively greater resistance to elvitegravir than raltegravir. Drug resistance could not be overcome by preincubating the drugs with IN, consistent with the binding of raltegravir and elvitegravir at the IN-DNA interface. Finally, we found an inverse correlation between resistance and catalytic activity of the IN mutants.


Marinello, Jessica; Marchand, Christophe; Mott, Bryan T; Bain, Anjali; Thomas, Craig; Pommier, Yves;


  • Amino Acid Substitution
  • Catalysis
  • DNA, Viral/ chemistry
  • DNA, Viral/ genetics
  • Drug Resistance, Viral/ drug effects
  • Drug Resistance, Viral/ genetics
  • HIV Integrase/ chemistry
  • HIV Integrase/ genetics
  • HIV Integrase Inhibitors/ chemistry
  • HIV Integrase Inhibitors/ pharmacology
  • HIV-1/ enzymology
  • HIV-1/ genetics
  • Mutation, Missense
  • Protein Binding/ drug effects
  • Protein Binding/ genetics
  • Pyrrolidinones/ chemistry
  • Pyrrolidinones/ pharmacology
  • Quinolones/ chemistry
  • Quinolones/ pharmacology
  • Raltegravir Potassium
  • Virus Replication/ drug effects
  • Virus Replication/ genetics

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