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Using H1299 wild-type cells and their MPND-knockout derivatives as research subjects, this project employs Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) for metabolic labeling of the two cell groups. Combined with ubiquitinated peptide-specific enrichment and nano-liquid chromatogra...
ORGANISM(S): Homo sapiens (Human) 
2026-05-15 | PXD074990 | Pride
he Mpr1/Pad1 N-terminal domain-containing protein (MPND) belongs to the JAMM family of deubiquitinases and is ubiquitously expressed across human tissues. However, its role in non-small cell lung cancer (NSCLC) remains unexplored. In this study, we demonstrate that MPND expression is frequently redu...
ORGANISM(S): Homo sapiens (Human) 
2026-05-15 | PXD067575 | Pride
In this study, H1975 wild-type and MPND-knockout cells were used for SILAC-based quantitative ubiquitin proteomics. Ubiquitinated peptides were enriched and analyzed by nano-LC-MS/MS. MaxQuant was used for protein quantification and differential ubiquitination site screening. Bioinformatic analyses ...
ORGANISM(S): Homo sapiens (Human) 
2026-08-18 | PXD082747 | Pride
Genomics
ATAC-seq analysis of differential peaks in parental and MPND knockout cells
Genomics
ChIP-seq analysis of differential H2B K120ub peaks in parental and MPND knockout cells
Genomics
ChIP-seq analysis of differential H2A K119ub peaks in parental and MPND knockout cells
Genomics
MPND loss in NSCLC drives tumor growth and metastasis by epigenetically activating TGF-beta/SMAD3 signaling
Genomics
RNA-sequencing of MPND wild-type and knockout mouse embryonic fibroblasts (MEFs) under basal conditions or upon IL-1beta or TNF-alpha stimulation
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