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Stable isotope labeling with amino acids in mouse xenografts.

ABSTRACT: This dataset corresponds to a SILAC analysis in mouse xenografts and in cell culture. We analysed signalling in tumors by means of a method based on stable isotope labeling with amino acids of xenograft tumors by the addition of [(13)C(6)]-lysine into mouse food, and also using a typical SILAC analysis in cell culture. This dataset includes 2 groups of analysis: one, with maxquant file tagged SILAX, corresponding to the xenograft analysis, the other one to SILAC analysis in cell culture. Data were acquired on an LTQ-Orbitrap XL mass spectrometer coupled with an Ultimate 3000 HPLC. Analysis was performed using MaxQuant software (version 1.1.1.36). All MS/MS spectra were searched using Andromeda against a database consisting of a combination of Homo sapiens and Mus musculus CPS databases and 250 classical contaminants. Search was performed allowing the following variable modifications: Oxidation (M) and Phospho (STY). FDR was set at 0.01 for peptides and proteins, and the minimal peptide length was six. Quantification was also performed using standard parameters; we considered only proteins with at least two identified/quantified peptides.

INSTRUMENT(S): LTQ Orbitrap

ORGANISM(S): Homo Sapiens (human) Mus Musculus (mouse)

SUBMITTER: Serge Urbach

LAB HEAD: Serge Urbach

PROVIDER: PXD000044 | Pride | 2013-01-17

REPOSITORIES: Pride

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			Action	DRS
	SILAX1_100709_A_G02_O1.RAW	Raw
	SILAX1_100709_A_G03_O1.RAW	Raw
	SILAX1_100709_A_G04_O1.RAW	Raw
	SILAX1_100709_A_G05_O1.RAW	Raw
	SILAX1_100709_A_G06_O1.RAW	Raw

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