Salt-dependent non-catalytic allostery of human USP14-regulated 26S proteasome

Abstract

USP14, a deubiquitylating enzyme, regulates 26S proteasome function both catalytically and non-catalytically through multiple checkpoints. How USP14 non-catalytically regulates the proteasome activity remains elusive. Here, we combined genetic engineering and cryo-EM to disentangle how USP14 non-catalytically regulates proteasome activity in a salt-dependent manner. By solving 16 high-resolution cryo-EM structures of substrate-engaged human 26S proteasome complexed with a catalytically deficient mutant USP14, we demonstrate that USP14s non-catalytic activity alone can induce parallel pathways of proteasome state transitions, leading to opposing substrate fates. The USP14 mutant allosterically reprograms the AAA-ATPase motor, inducing novel substrate-engaged conformations and filling major gaps in understanding asymmetric ATP-hydrolysis cycling around the ATPase ring. Time-resolved cryo-EM and functional analysis reveal that sodium or potassium promotes substrate-engaged pathways and suppresses USP14 activity for enhanced degradation, uncovering another layer of complexity in proteasome regulation.