The cotranslational cycle of the ribosome-bound Hsp70 homolog Ssb

Coupling of ribosomal translation with cotranslational protein folding is essential for cellular homeostasis. In eukaryotes, Hsp70 and its J-domain cochaperone, the heterodimeric ribosome-associated complex (RAC), are central to this process; however, mechanistic insights into the coordination of Hsp70 function with translation remain limited. Here, we present two cryo-EM structures of the ribosome-bound yeast Hsp70 Ssb, identifying Rpl25/uL23 as the ribosomal binding site and revealing its interaction with a model nascent chain. Together with detailed biochemical and mutational analyses, these structures enable us to delineate the intricate RAC-dependent cycle, which positions the substrate binding domain of Ssb-ATP close to the tunnel exit to receive nascent chains. This arrangement allows Ssb to undergo substantial conformational changes upon ATP hydrolysis without steric clashes with the ribosome, while the substrate binding domain of Ssb, now anchored by the tightly bound nascent chain, remains close to the tunnel exit.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2026-01-16
DOI
https://doi.org/10.1038/s41467-025-67685-6
Primary Topic
Heat shock proteins research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The cotranslational cycle of the ribosome-bound Hsp70 homolog Ssb

Volker Hübscher, Julia Schimpf, Sabine Rospert, Leonie Vollmar et al.
Nature Communications
Heat shock proteins research
article

The cotranslational cycle of the ribosome-bound Hsp70 homolog Ssb

Volker Hübscher, Julia Schimpf, Sabine Rospert, Leonie Vollmar, Irina Grishkovskaya, Thorsten Hugel, Lorenz Grundmann, Anna Moddemann, Mohd. Areeb, Kerstin Werner, Ying Zhang
article en

Abstract

Coupling of ribosomal translation with cotranslational protein folding is essential for cellular homeostasis. In eukaryotes, Hsp70 and its J-domain cochaperone, the heterodimeric ribosome-associated complex (RAC), are central to this process; however, mechanistic insights into the coordination of Hsp70 function with translation remain limited. Here, we present two cryo-EM structures of the ribosome-bound yeast Hsp70 Ssb, identifying Rpl25/uL23 as the ribosomal binding site and revealing its interaction with a model nascent chain. Together with detailed biochemical and mutational analyses, these structures enable us to delineate the intricate RAC-dependent cycle, which positions the substrate binding domain of Ssb-ATP close to the tunnel exit to receive nascent chains. This arrangement allows Ssb to undergo substantial conformational changes upon ATP hydrolysis without steric clashes with the ribosome, while the substrate binding domain of Ssb, now anchored by the tightly bound nascent chain, remains close to the tunnel exit.

Nature CommunicationsVol. 17(1)
University of Freiburg (DE), Research Institute of Molecular Pathology (AT), Vienna Biocenter (AT), Medical University of Vienna (AT)
Openalex Percentile: Top 87%
Heat shock proteins research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.