Related Experiment Video
Updated: Jan 12, 2026

Examining Proteasome Assembly with Recombinant Archaeal Proteasomes and Nondenaturing PAGE: The Case for a Combined Approach
Published on: December 17, 2016
Structural landscape of the degrading 26S proteasome reveals conformation-specific binding of TXNL1
Connor Arkinson1,2,3, Christine L Gee1,2,3, Zeyuan Zhang4
1California Institute for Quantitative Biosciences, University of California at Berkeley, Berkeley, CA, USA.
Abstract:
The 26S proteasome targets many cellular proteins for degradation during homeostasis and quality control. Proteasome-interacting cofactors modulate these functions and aid in substrate degradation. Here we solve high-resolution structures of the redox active cofactor TXNL1 bound to the human 26S proteasome at saturating and substoichiometric concentrations by time-resolved cryo-electron microscopy (cryo-EM). We identify distinct binding modes of TXNL1 that depend on the proteasome conformation and ATPase motor states. Together with biophysical and biochemical experiments, we show that the resting-state proteasome binds TXNL1 with low affinity and in variable positions on top of the Rpn11 deubiquitinase. In contrast, in the actively degrading proteasome, TXNL1 uses additional interactions for high-affinity binding, whereby its C-terminal tail covers the catalytic groove of Rpn11 and coordinates the active-site Zn2+. Furthermore, these cryo-EM structures of the degrading proteasome capture the ATPase hexamer in several spiral-staircase arrangements that indicate temporally asymmetric hydrolysis and conformational changes in bursts during mechanical substrate unfolding and translocation. Remarkably, we catch the proteasome in the act of unfolding the β-barrel mEos3.2 substrate while the ATPase hexamer is in a particular staircase register. Our findings advance current models for protein translocation through hexameric AAA+ motors and reveal how the proteasome uses its distinct conformational states to coordinate cofactor binding and substrate processing.
Insights
The 26S proteasome uses cofactor TXNL1 differently depending on its activity state. Time-resolved cryo-EM reveals how TXNL1 binds and regulates protein degradation and unfolding by the proteasome.
Area of Science:
- Molecular Biology
- Structural Biology
- Biochemistry
Background:
- The 26S proteasome is crucial for cellular protein degradation, homeostasis, and quality control.
- Proteasome-interacting cofactors dynamically regulate proteasome function and substrate degradation.
Purpose of the Study:
- To elucidate the high-resolution structures of the redox-active cofactor TXNL1 bound to the human 26S proteasome.
- To understand how TXNL1 binding varies with proteasome conformation and ATPase motor states.
Main Methods:
- Time-resolved cryo-electron microscopy (cryo-EM) at saturating and substoichiometric TXNL1 concentrations.
- Biophysical and biochemical experiments.
- High-resolution structure determination.
Main Results:
- Distinct TXNL1 binding modes were identified, dependent on proteasome conformation and ATPase activity.
- TXNL1 exhibits low-affinity binding in the resting-state proteasome and high-affinity binding in the actively degrading state, covering Rpn11's catalytic groove.
- Cryo-EM structures captured the proteasome unfolding a substrate (mEos3.2) and revealed ATPase hexamer dynamics during translocation.
Conclusions:
- The proteasome's distinct conformational states coordinate cofactor binding and substrate processing.
- Findings advance models of protein translocation through AAA+ motors.
- TXNL1 plays a key role in regulating proteasome-mediated protein degradation and unfolding.
Related Concept Videos
The Proteasome Structure
The proteasome is an...
The Proteasome
In this pathway, the target proteins are first tagged with small proteins called ubiquitin. A series of enzymes carry out the ubiquitination of the target proteins - E1 (ubiquitin-activating enzyme), E2 (ubiquitin-conjugating enzyme), and E3...
The Proteasome
In this pathway, the target proteins are first tagged with small proteins called ubiquitin. This involves participation of a series of enzymes including— E1 (ubiquitin-activating enzyme), E2 (ubiquitin-conjugating enzyme), and E3...
The Proteasome
Conserved Binding Sites
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
Translocation of Proteins into the Mitochondria
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...

