Proteomics

Dataset Information

0

LC-MS-Based Quantitative Proteomic Profiling Reveals WWQ-03-012-Induced Alterations in Protein Expression of Human HEL Cells


ABSTRACT: This experiment employs an analytical platform based on the Ultimate 3000 nano ultra-high-performance liquid chromatography system coupled to the Q Exactive Plus high-resolution mass spectrometer, combined with database search software, to conduct qualitative (or relative quantitative) analysis of proteins in samples from different experimental groups. The resulting protein list reflects the types and relative abundances of proteins detected in this mass spectrometry analysis.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Cell

DISEASE(S): Acute Leukemia

SUBMITTER: Mei Husheng  

LAB HEAD: Jing Yang

PROVIDER: PXD065708 | Pride | 2026-02-09

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
YAS202412200028-1-HEL-1.raw Raw
YAS202412200028-1-HEL-2.raw Raw
YAS202412200028-1-HEL-3.raw Raw
YAS202412200028-1-HEL03-1.raw Raw
YAS202412200028-1-HEL03-2.raw Raw
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Publications


The JAK2-V617F mutation is the most common genetic alteration in myeloproliferative neoplasms (MPN), which can progress to secondary acute myeloid leukemia (sAML), a chemotherapy-resistant disease with limited treatment options and a poor prognosis. Although the JAK1/2 inhibitor Ruxolitinib is clinically approved, its efficacy is limited by toxicity to normal cells and the development of drug resistance. Here, the deSUMOylase DESI2 is identified as a novel component of the JAK2-V617F complex by  ...[more]

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