SARS-CoV-2 S protein ACE2 interaction reveals novel allosteric targets

Raghuvamsi, Palur; Tulsian, Nikhil; Samsudin, Firdaus; Qian, Xinlei; Purushotorman, Kiren; Yue, Gu; Kozma, Mary; Lescar, Julien; Bond, Peter; MacAry, Paul; Anand, Ganesh

The Spike (S) protein is the main handle for SARS-CoV-2 to enter host cells through surface ACE2 receptors. How ACE2 binding activates proteolysis of S protein is unknown. Here, we have mapped the S:ACE2 interface and uncovered long-range allosteric propagation of ACE2 binding to sites critical for viral host entry. Unexpectedly, ACE2 binding enhances dynamics at a distal S1/S2 cleavage site and flanking protease docking site ~27 Ã… away while dampening dynamics of the stalk hinge (central helix and heptad repeat) regions ~ 130 Ã… away. This highlights that the stalk and proteolysis sites of the S protein are dynamic hotspots in the pre-fusion state. Our findings provide a mechanistic basis for S:ACE2 complex formation, critical for proteolytic processing and viral-host membrane fusion and highlight protease docking sites flanking the S1/S2 cleavage site, fusion peptide and heptad repeat 1 (HR1) as allosterically exposed cryptic hotspots for potential therapeutic development. One Sentence Summary SARS-CoV-2 spike protein binding to receptor ACE2 allosterically enhances furin proteolysis at distal S1/S2 cleavage sites