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We developed a novel approach to in situ crosslinking mass spectrometry (XL-MS) where the reaction is split into two sequential and orthogonal coupling events. The method involves pre-stabilization of the proteome using a fixation protocol, followed by a two-step process that begins with extensive l...
ORGANISM(S): Homo sapiens (Human) Escherichia coli 
2025-01-28 | PXD059118 | Pride
We used double-click-seq method to profile chromatin deposition bias in RPE-1 cells. Untreated wild-type, p53 knock-out and several treatments (hydroxyurea, ATR inhibitor, curaxin) and their combinations were profiled for characterizing assymetry during DNA replication.
ORGANISM(S): Homo sapiens 
Catechol estrogens (CEs) are metabolic electrophiles that actively undergo covalent interaction with cellular proteins, influencing molecular function. There is no feasible method to identify their binders in a living system. Herein, we developed a click chemistry-based approach using ethinylestradi...
ORGANISM(S): Rattus norvegicus (Rat) 
2022-02-28 | PXD009657 | Pride
We used double-click-seq and SCAR-seq methods to profile chromatin deposition bias in RPE-1 cells. Untreated cells and treatments promoting G4 formation (hydroxyurea, NMM) and their combination were profiled for characterizing chromatin protein redistribution asymmetry during DNA replication. This i...
ORGANISM(S): Homo sapiens 
Click-enabled analogues reveal pregnenolone interactomes in cancer and immune cells. TMT-6 experiment of tryptic, carbamidomethylated peptides of mouse CD8+ T-cells after protein pull-down on pregnenolone beads.
ORGANISM(S): Mus musculus (Mouse) 
2021-04-26 | PXD025574 | Pride
Rna_seq analysis of muscle in click and EDC treated mouse
The success of targeted therapies hinges on our ability to understand the molecular and cellular mechanism of action of these agents. Here we modify various BET bromodomain inhibitors, an exemplar novel targeted therapy, to create functionally conserved compounds that are amenable to click-chemistry...
ORGANISM(S): Homo sapiens 
2017-07-13 | GSE88749 | GEO
The success of targeted therapies hinges on our ability to understand the molecular and cellular mechanism of action of these agents. Here we modify various BET bromodomain inhibitors, an exemplar novel targeted therapy, to create functionally conserved compounds that are amenable to click-chemistry...
ORGANISM(S): Homo sapiens 
2017-07-13 | GSE88748 | GEO
Identification of newly synthesized proteins in microbial communities using BONCAT and click chemistry
Double-click-seq allows to track new histone deposition bias in hRPE-1 cells
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