Ron Geller

This study investigates the functional role of the SARS-CoV-2 Spike protein transmembrane domain in viral entry and identifies key sequence and structural features critical for its activity.

This study examines deletion repair in the BA.1 SARS-CoV-2 spike protein, finding that such events are rare and have limited direct impact on viral evolution but may influence fitness-enhancing mutations.

The paper maps mutation tolerability across a viral proteome, revealing structural and functional correlates and implications for drug target selection.

This paper describes an efficient plasmid-based system for producing recombinant VSV encoding foreign glycoproteins, validated with glycoproteins from multiple viral families.

This study shows how SARS-CoV-2 spike protein adapts to different human cell types through mutations that affect entry efficiency and receptor affinity.

The paper investigates the structural and functional impact of the S:A222V mutation in SARS-CoV-2, showing increased RBD opening and ACE2 binding without reducing neutralization capacity.