| Literature DB >> 27090931 |
Nese Kurt Yilmaz1, Ronald Swanstrom2, Celia A Schiffer3.
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.Entities:
Keywords: HIV-1 protease; drug resistance; protease inhibitors; resistance mutations; structure-based drug design; substrate envelope
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Year: 2016 PMID: 27090931 PMCID: PMC4912444 DOI: 10.1016/j.tim.2016.03.010
Source DB: PubMed Journal: Trends Microbiol ISSN: 0966-842X Impact factor: 17.079