[PDF][PDF] Mitochondrial ClpP-mediated proteolysis induces selective cancer cell lethality
…, O Halgas, T Nii, Y Jitkova, R Zhao, J St-Germain… - Cancer cell, 2019 - cell.com
The mitochondrial caseinolytic protease P (ClpP) plays a central role in mitochondrial protein
quality control by degrading misfolded proteins. Using genetic and chemical approaches, …
quality control by degrading misfolded proteins. Using genetic and chemical approaches, …
[HTML][HTML] Global proteomic assessment of the classical protein-tyrosine phosphatome and “Redoxome”
…, M Fernandez, P Taylor, C Virtanen, JR St-Germain… - Cell, 2011 - cell.com
Protein-tyrosine phosphatases (PTPs), along with protein-tyrosine kinases, play key roles in
cellular signaling. All Class I PTPs contain an essential active site cysteinyl residue, which …
cellular signaling. All Class I PTPs contain an essential active site cysteinyl residue, which …
[HTML][HTML] Global interactomics uncovers extensive organellar targeting by Zika virus
…, BJA Dyakov, EMN Laurent, J St-Germain… - Molecular & Cellular …, 2018 - ASBMB
Zika virus (ZIKV) is a membrane enveloped Flavivirus with a positive strand RNA genome,
transmitted by Aedes mosquitoes. The geographical range of ZIKV has dramatically …
transmitted by Aedes mosquitoes. The geographical range of ZIKV has dramatically …
A SARS-CoV-2–host proximity interactome
Viral replication is dependent on interactions between viral polypeptides and host proteins.
Identifying virus-host protein interactions can thus uncover unique opportunities for …
Identifying virus-host protein interactions can thus uncover unique opportunities for …
[HTML][HTML] Tyrosyl phosphorylation of KRAS stalls GTPase cycle via alteration of switch I and II conformation
…, N Radulovich, BPK Poon, J St-Germain… - Nature …, 2019 - nature.com
Deregulation of the RAS GTPase cycle due to mutations in the three RAS genes is commonly
associated with cancer development. Protein tyrosine phosphatase SHP2 promotes RAF-to…
associated with cancer development. Protein tyrosine phosphatase SHP2 promotes RAF-to…
[HTML][HTML] RNF168 regulates R-loop resolution and genomic stability in BRCA1/2-deficient tumors
…, B Ho, S Duan, J St-Germain… - The Journal of …, 2021 - Am Soc Clin Investig
Germline mutations in BRCA1 and BRCA2 (BRCA1/2) genes considerably increase breast
and ovarian cancer risk. Given that tumors with these mutations have elevated genomic …
and ovarian cancer risk. Given that tumors with these mutations have elevated genomic …
[HTML][HTML] The Q61H mutation decouples KRAS from upstream regulation and renders cancer cells resistant to SHP2 inhibitors
T Gebregiworgis, Y Kano, J St-Germain… - Nature …, 2021 - nature.com
Cancer cells bearing distinct KRAS mutations exhibit variable sensitivity to SHP2 inhibitors (SHP2i).
Here we show that cells harboring KRAS Q61H are uniquely resistant to SHP2i, and …
Here we show that cells harboring KRAS Q61H are uniquely resistant to SHP2i, and …
A SARS-CoV-2 BioID-based virus-host membrane protein interactome and virus peptide compendium: new proteomics resources for COVID-19 research
JR St-Germain, A Astori, P Samavarchi-Tehrani… - BioRxiv, 2020 - biorxiv.org
Key steps of viral replication take place at host cell membranes, but the detection of
membrane-associated protein-protein interactions using standard affinity-based approaches (eg …
membrane-associated protein-protein interactions using standard affinity-based approaches (eg …
C5orf51 is a component of the MON1-CCZ1 complex and controls RAB7A localization and stability during mitophagy
BR Yan, T Li, E Coyaud, EMN Laurent, J St-Germain… - Autophagy, 2022 - Taylor & Francis
Depolarized mitochondria can be degraded via mitophagy, a selective form of autophagy.
The RAB GTPase RAB7A was recently shown to play a key role in this process. RAB7A …
The RAB GTPase RAB7A was recently shown to play a key role in this process. RAB7A …
[PDF][PDF] Mutations of the transcriptional corepressor ZMYM2 cause syndromic urinary tract malformations
…, E Coyaud, EMN Laurent, JR St-Germain… - The American Journal of …, 2020 - cell.com
Congenital anomalies of the kidney and urinary tract (CAKUT) constitute one of the most
frequent birth defects and represent the most common cause of chronic kidney disease in the …
frequent birth defects and represent the most common cause of chronic kidney disease in the …