Improving Viral Protease Inhibitors to Counter Drug Resistance

Trends Microbiol. 2016 Jul;24(7):547-557. doi: 10.1016/j.tim.2016.03.010. Epub 2016 Apr 15.

Abstract

Drug resistance is a major problem in health care, undermining therapy outcomes and necessitating novel approaches to drug design. Extensive studies on resistance to viral protease inhibitors, particularly those of HIV-1 and hepatitis C virus (HCV) protease, revealed a plethora of information on the structural and molecular mechanisms underlying resistance. These insights led to several strategies to improve viral protease inhibitors to counter resistance, such as exploiting the essential biological function and leveraging evolutionary constraints. Incorporation of these strategies into structure-based drug design can minimize vulnerability to resistance, not only for viral proteases but for other quickly evolving drug targets as well, toward designing inhibitors one step ahead of evolution to counter resistance with more intelligent and rational design.

Keywords: HIV-1 protease; drug resistance; protease inhibitors; resistance mutations; structure-based drug design; substrate envelope.

Publication types

  • Review
  • Research Support, N.I.H., Extramural

MeSH terms

  • Drug Design*
  • Drug Resistance, Viral / drug effects
  • HIV Infections / drug therapy*
  • HIV Protease / drug effects
  • Hepatitis C / drug therapy*
  • Humans
  • Protease Inhibitors / therapeutic use*

Substances

  • Protease Inhibitors
  • HIV Protease
  • p16 protease, Human immunodeficiency virus 1