New Zika virus inhibitor identified
Sanford-Burnham Medical Research Institute News May 25, 2017
Compound could serve as basis for drugs to prevent neurological complications of Zika.
New research led by Alexey Terskikh, PhD, associate professor at Sanford Burnham Prebys Medical Discovery Institute (SBP), and Alex Strongin, PhD, professor at SBP, could be a first step toward a drug to treat Zika infections.
The research findings were publishing in the journal Antiviral Research.
ÂWe identified a small molecule that inhibits the Zika virus protease, and show that it blocks viral propagation in human cells and in mice, Terskikh says. ÂAnti–Zika drugs are desperately needed. The fact that the compound seems to work in vivo is really promising, so we plan to use it as a starting point to make an even more potent and effective drug.Â
ÂMicrocephaly is likely just the tip of the iceberg in terms of the potential adverse effects of maternal Zika infection, comments Terskikh. ÂThere may be other, less obvious impacts on brain development that wouldnÂt be apparent until later. ThatÂs something weÂre also investigating.Â
The scientific team took advantage of a library of compounds that StronginÂs lab had previously shown to inhibit the same component of the related West Nile virus. They also tested structurally similar molecules available at the SBPÂs Conrad Prebys Center for Chemical Genomics (Prebys Center) to determine whether any also blocked the protease.
The screening process identified three promising compounds, which were then tested for their ability to prevent Zika infection of human brain cells. The best one of these also reduced the amount of virus circulating in the blood of Zika–infected mice.
ÂThe inhibitorÂs efficacy in animals is the key to the studyÂs significance, Terskikh adds. ÂThis, and the fact that the compound is likely to be safe make it especially promising. The compound blocks a part of the protease thatÂs unique to viruses, so it doesnÂt inhibit similar human proteases. ItÂs also much more potent than previously identified inhibitors of the Zika protease.Â
This future drug is just one part of the fight against Zika. An experimental vaccine is set to move into phase 2 clinical trials in June.
ÂIn addition to a Zika vaccine, we still need antivirals, explains Terskikh. ÂSome people may be exposed who havenÂt been vaccinated. Having a way to treat the infection could help stop Zika from spreading and prevent its sometimes devastating effects.Â
This research was performed in collaboration with scientists at the La Jolla Institute for Allergy & Immunology.
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New research led by Alexey Terskikh, PhD, associate professor at Sanford Burnham Prebys Medical Discovery Institute (SBP), and Alex Strongin, PhD, professor at SBP, could be a first step toward a drug to treat Zika infections.
The research findings were publishing in the journal Antiviral Research.
ÂWe identified a small molecule that inhibits the Zika virus protease, and show that it blocks viral propagation in human cells and in mice, Terskikh says. ÂAnti–Zika drugs are desperately needed. The fact that the compound seems to work in vivo is really promising, so we plan to use it as a starting point to make an even more potent and effective drug.Â
ÂMicrocephaly is likely just the tip of the iceberg in terms of the potential adverse effects of maternal Zika infection, comments Terskikh. ÂThere may be other, less obvious impacts on brain development that wouldnÂt be apparent until later. ThatÂs something weÂre also investigating.Â
The scientific team took advantage of a library of compounds that StronginÂs lab had previously shown to inhibit the same component of the related West Nile virus. They also tested structurally similar molecules available at the SBPÂs Conrad Prebys Center for Chemical Genomics (Prebys Center) to determine whether any also blocked the protease.
The screening process identified three promising compounds, which were then tested for their ability to prevent Zika infection of human brain cells. The best one of these also reduced the amount of virus circulating in the blood of Zika–infected mice.
ÂThe inhibitorÂs efficacy in animals is the key to the studyÂs significance, Terskikh adds. ÂThis, and the fact that the compound is likely to be safe make it especially promising. The compound blocks a part of the protease thatÂs unique to viruses, so it doesnÂt inhibit similar human proteases. ItÂs also much more potent than previously identified inhibitors of the Zika protease.Â
This future drug is just one part of the fight against Zika. An experimental vaccine is set to move into phase 2 clinical trials in June.
ÂIn addition to a Zika vaccine, we still need antivirals, explains Terskikh. ÂSome people may be exposed who havenÂt been vaccinated. Having a way to treat the infection could help stop Zika from spreading and prevent its sometimes devastating effects.Â
This research was performed in collaboration with scientists at the La Jolla Institute for Allergy & Immunology.
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