Abstract

The Sec translocon provides the lipid bilayer entry for ribosome‐bound nascent chains and thus facilitates membrane protein biogenesis. Despite the appreciated role of the native environment in the translocon:ribosome assembly, structural information on the complex in the lipid membrane is scarce. Here, we present a cryo‐electron microscopy‐based structure of bacterial translocon SecYEG in lipid nanodiscs and elucidate an early intermediate state upon insertion of the FtsQ anchor domain. Insertion of the short nascent chain causes initial displacements within the lateral gate of the translocon, where α‐helices 2b, 7, and 8 tilt within the membrane core to “unzip” the gate at the cytoplasmic side. Molecular dynamics simulations demonstrate that the conformational change is reversed in the absence of the ribosome, and suggest that the accessory α‐helices of SecE subunit modulate the lateral gate conformation. Site‐specific cross‐linking validates that the FtsQ nascent chain passes the lateral gate upon insertion. The structure and the biochemical data suggest that the partially inserted nascent chain remains highly flexible until it acquires the transmembrane topology.

Highlights

  • Membrane proteins constitute a large part of the cellular proteome and determine the vital functionality and identity of biological membranes

  • A 2019 The Authors analysis, we resolved for the first time all three subunits of SecYEG in nanodiscs and described a novel conformation, where SecY transmembrane a-helices (TMHs) 2b and 7 were apart at the cytoplasmic side to form a V-shaped lateral gate that is pre-opened for the nascent chain insertion, while accessory SecE TMHs 1 and 2 interacted with the gate at the periplasmic side

  • Functional reconstitution of E. coli SecYEG in nanodiscs has been previously performed by several groups for biochemical, biophysical, and structural studies and allowed probing of the translocon interactions with the motor protein SecA, targeting factors, and ribosomes [14,20,24,25]

Read more

Summary

Introduction

Membrane proteins constitute a large part of the cellular proteome and determine the vital functionality and identity of biological membranes. A compact “primed” state has been described for detergent-solubilized translocons in the absence of hydrophobic nascent chains [11], while a recent cryo-electron tomography analysis has revealed a predominantly open conformation of the ribosome-bound Sec61 within native ER membranes and so suggested a crucial effect of the molecular environment on protein dynamics [23].

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call