AI‑driven protein design creates potent anti‑CRISPR inhibitors that block Cas13 activity, offering a new potential tool for safer, more controlled gene editing.
A GIF showing a protein mimicking IL-2 binding to IL-2 receptors, then changing shape in response to an effector molecule, which forces it off of one of the receptors. A protein mimicking IL-2 called ...
“Proteins float around in the cell and constantly bump into each other. How can you design rates at which biology happens fast?” Adam Broerman, a graduate student at the University of Washington (UW), ...
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