Fri 06 November 2020:
Scientists identify promising candidate to combat COVID-19.
By screening hundreds of synthetic mini-antibodies called sybodies, a group of scientists has identified one that might stop SARS-CoV-2 from infecting human cells. Using DESY’s X-ray light source PETRA III, the team could unravel how the sybody interacts with the virus. The scientists from the Hamburg branch of the European Molecular Biology Laboratory EMBL, the Centre for Structural Systems Biology CSSB at DESY and other institutions report their findings in the journal Nature Communications.
The ability of SARS-CoV-2 to infect cells depends on interactions between the viral spike protein and the human cell surface protein ACE2. To enable the virus to hook onto the cell surface, the spike protein binds ACE2 using three finger-like protrusions, called the receptor binding domains (RBDs). Blocking the RBDs therefore has the potential to stop the virus from entering human cells. This can be done using antibodies.
Nanobodies, small antibodies found in camels and llamas, are promising as tools against viruses due to their high stability and small size. Although obtaining them from animals is time consuming, technological advances now allow for rapid selection of synthetic nanobodies, called sybodies. A technology platform to select sybodies from large synthetic libraries was recently developed in the lab of Markus Seeger at the University of Zurich, and made available for this study.
EMBL Hamburg’s Christian Löw group searched through the existing libraries to find sybodies that could block SARS-CoV-2 from infecting human cells. First, they used the viral spike protein’s RBDs as bait to select those sybodies that bind to them. Next, they tested the selected sybodies according to their stability, effectiveness, and the precision of binding. Among the best binders, one called sybody 23 turned out to be particularly effective in blocking the RBDs.
To learn exactly how sybody 23 interacts with the viral RBDs, researchers in the group of Dmitri Svergun at EMBL Hamburg analysed the binding of sybody 23 to the RBDs by small-angle X-ray scattering at DESY’s X-ray source PETRA III. In addition, Martin Hällberg at CSSB and Karolinska Institutet in Stockholm used a special electron microscope working at low temperatures (cryo-EM) to determine the structure of the full SARS-CoV-2 spike bound to sybody 23. The RBDs switch between two positions: in the ‘up’ position the RBDs poke out, ready to bind ACE2; in the ‘down’ position they are furled to hide from the human immune system. The molecular structures revealed that sybody 23 binds RBDs in both ‘up’ and ‘down’ positions, and blocks the areas where ACE2 would normally bind. This ability to block RBDs regardless of their position might explain why sybody 23 is so effective.
Finally, to test if sybody 23 can neutralise a virus, the group of Ben Murrell at Karolinska Institutet used a different virus, called a lentivirus, modified such that it carried SARS-CoV-2’s spike protein on its surface. They observed that sybody 23 successfully disabled the modified virus in vitro. Additional tests will be necessary to confirm whether this sybody could stop SARS-CoV-2 infection in the human body. The results of this project hold out the promise of a potential way to treat COVID-19. In future work, the scientists will perform further analyses to confirm whether sybody 23 could be an effective COVID-19 treatment.
This article was originally published in Technology.org CLICK HERE
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