Proteomics

Dataset Information

0

Identification of novel Coronin 1A interacting proteins


ABSTRACT: Severe combined immunodeficiency 8 (IMD8) is caused by mutations in the human Coronin 1A (Coro1A). The clinical presentation of IMD8 patients is characterized by recurrent bacterial infections, suggesting an important role of Coro1A in innate immunity. To analyze the molecular mechanism of Coro1A during neutrophil recruitment, we identified the Coro1A interactome by conducting co-immunoprecipitation (Co-IP) experiments using GFP NanoTrap technology and subsequent mass spectrometry (LC-MS/MS) using human neutrophil-like differentiated HL-60 (dHL-60) cells stably expressing Coro1A-EGFP (dHL-60-Coro1A-EGFP) cells.

INSTRUMENT(S): LTQ Orbitrap

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Leukocyte

SUBMITTER: Ignasi Forne  

LAB HEAD: Barbara Walzog

PROVIDER: PXD004635 | Pride | 2017-06-29

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
MaxQuant_Output.zip Other
Ref538_191115_sample01.raw Raw
Ref538_191115_sample02.raw Raw
Ref538_191115_sample03.raw Raw
Ref538_191115_sample04.raw Raw
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Publications


Trafficking of polymorphonuclear neutrophils (PMNs) during inflammation critically depends on the β<sub>2</sub> integrins lymphocyte function-associated antigen 1 (LFA-1) (CD11a/CD18) and macrophage-1 antigen (CD11b/CD18). Here, we identify coronin 1A (Coro1A) as a novel regulator of β<sub>2</sub> integrins that interacts with the cytoplasmic tail of CD18 and is crucial for induction of PMN adhesion and postadhesion events, including adhesion strengthening, spreading, and migration under flow co  ...[more]

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