| Literature DB >> 28584151 |
David Wensel1, Yongnian Sun2, Zhufang Li2, Sharon Zhang2, Caryn Picarillo3, Thomas McDonagh3, David Fabrizio2, Mark Cockett2, Mark Krystal2, Jonathan Davis3.
Abstract
A novel fibronectin-based protein (Adnectin) HIV-1 inhibitor was generated using in vitro selection. This inhibitor binds to human CD4 with a high affinity (3.9 nM) and inhibits viral entry at a step after CD4 engagement and preceding membrane fusion. The progenitor sequence of this novel inhibitor was selected from a library of trillions of Adnectin variants using mRNA display and then further optimized for improved antiviral and physical properties. The final optimized inhibitor exhibited full potency against a panel of 124 envelope (gp160) proteins spanning 11 subtypes, indicating broad-spectrum activity. Resistance profiling studies showed that this inhibitor required 30 passages (151 days) in culture to acquire sufficient resistance to result in viral titer breakthrough. Resistance mapped to the loss of multiple potential N-linked glycosylation sites in gp120, suggesting that inhibition is due to steric hindrance of CD4-binding-induced conformational changes.Entities:
Keywords: Adnectin; CD4; HIV inhibitor; N17; gp41; human immunodeficiency virus
Mesh:
Substances:
Year: 2017 PMID: 28584151 PMCID: PMC5527662 DOI: 10.1128/AAC.00508-17
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191