Proteomics

Dataset Information

0

Identification of novel constituents of ALIS from macrophage lysates (LPS+/-), LC MS/MS


ABSTRACT: Macrophages assemble aggresome-like induced structures or ALIS upon LPS or E. coli mediated TLR4 stimulation. These structures are positive for p62, LC3 and ubiquitinated proteins, form irrespective of autophagy, and persist within the cell system up to 48h. However, their composition is not well known. Our aim was to identify proteins constituting ALIS and establish its functionality in host-defense response under infectious conditions.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Cell Culture, Macrophage

SUBMITTER: Srinivasa Srinivasula  

LAB HEAD: Srinivasa Murty Srinivasula

PROVIDER: PXD031163 | Pride | 2024-05-23

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
66534-_1_.mzML Mzml
66534-_1_.pdResult Other
All_Proteins.mgf Mgf
LPS_treated_fraction_25.raw Raw
LPS_treated_fraction_26.raw Raw
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Publications

TLR-mediated aggresome-like induced structures comprise antimicrobial peptides and attenuate intracellular bacterial survival.

Bhatnagar Anushree A   Chopra Umesh U   Raja Sebastian S   Das Krishanu Dey KD   Mahalingam S S   Chakravortty Dipshikha D   Srinivasula Srinivasa Murty SM  

Molecular biology of the cell 20240103 3


Immune cells employ diverse mechanisms for host defense. Macrophages, in response to TLR activation, assemble aggresome-like induced structures (ALIS). Our group has shown TLR4-signaling transcriptionally upregulates p62/sequestome1, which assembles ALIS. We have demonstrated that TLR4-mediated autophagy is, in fact, selective-autophagy of ALIS. We hypothesize that TLR-mediated autophagy and ALIS contribute to host-defense. Here we show that ALIS are assembled in macrophages upon exposure to dif  ...[more]

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