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Keyword
- aa1
- amino acids1
- cBAF complex1
- coefficient of variation1
- CV1
- ELISA1
- enzyme-linked immunosorbent assay1
- ERG1
- ERG interactome1
- ERG protein isoforms1
- FFPE1
- formalin-fixed paraffin-embedded tissues1
- IHC1
- immunohistochemistry1
- label-free quantification1
- LC-MS/MS1
- LFQ1
- liquid chromatography-tandem mass spectrometry1
- PCa1
- PRM1
- RT1
- SRM1
- TMPRSS2-ERG fusion1
- VCaP1
April 2021 Issue
1 Results
- ResearchOpen Access
Mapping Isoform Abundance and Interactome of the Endogenous TMPRSS2-ERG Fusion Protein by Orthogonal Immunoprecipitation–Mass Spectrometry Assays
Molecular & Cellular ProteomicsVol. 20100075Published online: March 22, 2021- Zhiqiang Fu
- Yasmine Rais
- Tarek A. Bismar
- M. Eric Hyndman
- X. Chris Le
- Andrei P. Drabovich
Cited in Scopus: 0In Brief Orthogonal immunoprecipitation-mass spectrometry assays quantified TMPRSS2-ERG fusion protein (∼27,000 copies/cell) and its four distinct isoforms, and revealed that T1E4-ERG isoform accounted for 52 ± 3% of the total ERG in VCaP cells and 50 ± 11% in FFPE prostate cancer tissues. Methionine-truncated and N-acetylated peptide TASSSSDYGQTSK unique for T1/E4 TMPRSS2-ERG fusion was identified. Unlike the N-terminal antibodies, C-terminal antibodies identified 29 ERG-interacting proteins, including mutually exclusive BRG1- and BRM-associated canonical SWI/SNF chromatin remodeling complexes. Clinical perspectives of assays were discussed.