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Small Molecules Target Entry Mechanism for Deadly Viruses

New drug target for Ebola, Marburg viruses

 E-Mail IMAGE: UIC s Lijun Rong is part of a team of UIC researchers who have identified a previously unknown site on filoviruses a type of virus, like Ebola, that causes hemorrhagic. view more  Credit: Jenny Fontaine/UIC Ebola and Marburg are among the most deadly viruses, with mortality rates from these infections ranging from 25% to 90%. While no drugs currently are available on the market to prevent infection from these viruses they belong to a category of viruses called filoviruses, which are known to cause hemorrhagic fever researchers have identified a few small drug molecules that can block filoviruses from infecting cells by occupying a single site on a glycoprotein in the virus.

Researchers develop boosters to train immune responses against Covid-19

February 04, 2021 × The new approach allows a dramatic shortening of the response time upon real infections, which can be critical in certain patients Researchers at the University of Illinois Chicago and California State University in Sacramento, US have found an alternative approach to train immune responses against Covid-19. They have developed a novel strategy that redirects antibodies for other diseases existing in humans to the spike proteins of SARS-CoV-2. The team proposes using peptide-based double-faced “booster” inhibitors, with one face binding to the spike proteins of SARS-CoV-2 and the other face binding to generic hepatitis B antibodies. “Once the SARS-CoV-2 viruses become labelled by the hepatitis B antibodies via intermediate boosters, the viruses will be neutralised,” said Petr Král, UIC Professor of chemistry, physics, pharmaceutical sciences and senior author on the paper.

Novel strategy redirects generic antibodies to SARS-CoV-2 spike proteins

Novel strategy redirects generic antibodies to SARS-CoV-2 spike proteins The SARS-CoV-2, the new coronavirus behind the current pandemic, infects humans by binding its surface-exposed spike proteins to ACE2 receptors exposed on the cell membranes. Upon a vaccination or a real infection, it takes several weeks before the immunity develops antibodies that can selectively bind to these spike proteins. Such antibody-labeled viruses are neutralized by the natural killer and T cells operated by the human immunity. An alternative approach to train the immunity response is offered by researchers at the University of Illinois Chicago and California State University at Sacramento who have developed a novel strategy that redirects antibodies for other diseases existing in humans to the spike proteins of SARS-CoV-2.

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