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Improving Viral Protease Inhibitors to Counter Drug Resistance

Journal

TRENDS IN MICROBIOLOGY
Volume 24, Issue 7, Pages 547-557

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.tim.2016.03.010

Keywords

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Funding

  1. National Institute of Health (NIH) [P01 GM109767, R01 AI085051]

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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.

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