Rui Pedro Galão

This study designs sulfonated polymersomes that inhibit multiple viruses by targeting host cell receptors, showing potent in vitro and in vivo antiviral activity.

This study identifies how the long ZAP isoform recruits enzymes to degrade viral RNA through a coordinated decay pathway.

The paper identifies diverse spike haplotypes in persistent SARS-CoV-2 infections that show immune escape mechanisms similar to variants of concern.

The paper identifies KHNYN as a novel ZAP cofactor essential for restricting HIV-1 with clustered CpG dinucleotides.