Structural Basis of CYRI-B Direct Competition with Scar/WAVE Complex for Rac1

Rac1 is a major regulator of actin dynamics, with GTP-bound Rac1 promoting actin assembly via the Scar/WAVE complex. CYRI competes with Scar/WAVE for interaction with Rac1 in a feedback loop regulating actin dynamics. Here, we reveal the nature of the CYRI-Rac1 interaction, through crystal structures of CYRI-B lacking the N-terminal helix (CYRI-BDN) and the CYRI-BDN:Rac1Q61L complex, providing the molecular basis for CYRI-B regulation of the Scar/WAVE complex. We reveal CYRI-B as having two subdomains - an N-terminal Rac1 binding subdomain with a unique Rac1-effector interface and a C-terminal Ratchet subdomain that undergoes conformational changes induced by Rac1 binding. Finally, we show that the CYRI protein family, CYRI-A and CYRI-B can produce an autoinhibited hetero- or homodimers, adding an additional layer of regulation to Rac1 signaling.

Automated summary

Crystal structures of CYRI-B lacking the N-terminal helix (CYRI-BDN) and the CYRI-BDN:Rac1Q61L complex provide insights into the nature of CYRI-Rac1 interaction and the molecular basis of CYRI-B regulation of the Scar/WAVE complex. CYRI protein family can form autoinhibited hetero- or homodimers, adding an additional layer of regulation to Rac1 signaling pathways.