Proteomics

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Use of a modified Multiplexed Inhibitor Bead assay to study kinome responses to cytostatic treatment in human cancer cell lines Triplicate Test: pilot study


ABSTRACT: In order to improve elution of proteins from the column, to reduce the cost as well as the hands on time of the analysis, we here present a modification of the Multiplexed Inhibitor Bead assay (MIB assay), where we elute the proteins from beads containing covalently bound inhibitors using trypsin digestion. Three human cancer cell lines treated with the same chemotherapeutics, cisplatin and docetaxel, were used to monitor and evaluate the performance of the assay. Using this method, we see a good coverage of the kinome as well as other important signaling proteins using only three kinase inhibitors. We demonstrate that the method is reproducible and that the column is re-usable for more than 10 times without loss in performance. The MIB assay revealed large differences in the cellular signaling responses between the cell lines.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

SUBMITTER: Voin Petrovic  

PROVIDER: MSV000080744 | MassIVE | Wed Mar 29 05:01:00 BST 2017

SECONDARY ACCESSION(S): PXD005402

REPOSITORIES: MassIVE

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On-column trypsinization allows for re-use of matrix in modified multiplexed inhibitor beads assay.

Petrovic Voin V   Olaisen Camilla C   Sharma Animesh A   Nepal Anala A   Bugge Steffen S   Sundby Eirik E   Hoff Bård Helge BH   Slupphaug Geir G   Otterlei Marit M  

Analytical biochemistry 20170203


The Multiplexed Inhibitor Bead (MIB) assay is a previously published quantitative proteomic MS-based approach to study cellular kinomes. A rather extensive procedure, need for multiple custom-made kinase inhibitors and an inability to re-use the MIB-columns, has limited its applicability. Here we present a modified MIB assay in which elution of bound proteins is facilitated by on-column trypsinization. We tested the modified MIB assay by analyzing extract from three human cancer cell lines treat  ...[more]

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