Proteomics

Dataset Information

0

Analysis of Tim-3 interactome in primary mouse CD4+ T cells


ABSTRACT: We analyzed the interactome of the Tim-3 (HAVCR2) protein, using an affinity purification method based on the the endogenous expression of a One-Strep-tagged (OST) version of Tim-3 in an engineered mouse model, and affinity purification of the protein from expanded primary CD4+ T cells. Affinity purification of the OST tagged protein was performed using Streptactin beads, from T cells either non stimulated, or stimulated 30s, 120s, 300s or 900s with pervanadate. Each AP-MS purification is associated with a corresponding control (purification from CD4+ T cells isolated from WT mice, cultured and stimulated in the same conditions). The number of replicate biological experiments was n=3 for all conditions (time-points), and each sample was analyzed twice by nanoLC-MS, resulting in 60 raw files.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Spleen, Primary Cell, T Cell, Lymph Node

SUBMITTER: Anne Gonzalez de Peredo  

LAB HEAD: Odile Schiltz

PROVIDER: PXD020156 | Pride | 2022-06-30

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
OEMMA180629_01.raw Raw
OEMMA180629_03.raw Raw
OEMMA180629_05.raw Raw
OEMMA180629_07.raw Raw
OEMMA180629_09.raw Raw
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Publications

Opposing regulatory functions of the TIM3 (HAVCR2) signalosome in primary effector T cells as revealed by quantitative interactomics.

Zhai Yunhao Y   Celis-Gutierrez Javier J   Voisinne Guillaume G   Mori Daiki D   Girard Laura L   Burlet-Schiltz Odile O   de Peredo Anne Gonzalez AG   Roncagalli Romain R   Malissen Bernard B  

Cellular & molecular immunology 20201102 6


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