PXD054296 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Re-localization of components of the guided entry of tail-anchored proteins targeting pathway to cytosolic foci upon glucose starvation |
Description | Protein targeting is an essential step in the biogenesis of membrane proteins and the guided-entry of tail-anchored proteins (GET) pathway is a key targeting route to the endoplasmic reticulum. The adaptive response to cellular stress is multifaceted but a hallmark is the formation of membraneless organelles, which can act as sequestration sites for particular factors, allowing regulation of cellular processes during stress and/or facilitating efficient recovery upon stress alleviation. Upon glucose withdrawal, we observe that the Get3 ATPase of the GET pathway re-locates to dynamic cytosolic foci, here termed GET bodies, that also contain proteins of the GET pathway pre-targeting complex. Our data demonstrate that Get3 and the Get4-Get5 heterodimer play important roles in the assembly of these structures, and we further uncover the requirement of the TPR domain of Sgt2 for the GET body formation. Compositional analyses of GET bodies by enrichment coupled to mass spectrometry as well as high-throughput microscopy-based screening reveal a chaperone-rich core and the association of an inventory of proteins involved in metabolic processes. Temporal analyses of GET body assembly demonstrate the sequential recruitment of different chaperones and we discover the requirement of the co-chaperones Sis1 and Sti1 for maintaining the dynamic properties of these structures. As lack of Adh2, which converts ethanol to acetaldehyde in a reaction coupled to NADH production, impairs GET body disassembly, and the addition of NADH promotes GET body dissolution in vitro, our results suggest a mechanistic basis for the formation of GET bodies in response to the metabolic shift caused by glucose withdrawal. |
HostingRepository | PRIDE |
AnnounceDate | 2025-02-25 |
AnnouncementXML | Submission_2025-02-25_10:01:32.474.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Christof Lenz |
SpeciesList | scientific name: Saccharomyces cerevisiae (Baker's yeast); NCBI TaxID: 4932; |
ModificationList | No PTMs are included in the dataset |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-07-27 09:51:52 | ID requested | |
⏵ 1 | 2025-02-25 10:01:32 | announced | |
Publication List
Keyword List
submitter keyword: GET pathway, membrane proteins |
Contact List
Christof Lenz |
contact affiliation | University Medical Center Goettingen, Department of Clinical Chemistry, Core Facility Proteomics |
contact email | christof.lenz@med.uni-goettingen.de |
lab head | |
Christof Lenz |
contact affiliation | Max Planck Institute for Biophysical Chemistry |
contact email | christof.lenz@mpibpc.mpg.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD054296
- Label: PRIDE project
- Name: Re-localization of components of the guided entry of tail-anchored proteins targeting pathway to cytosolic foci upon glucose starvation